Pseudobulbar affect …

Fardin Nabizadeh MD

General Neurology

Updated 06.26.2024
Released 08.19.2002
Expires For CME 06.26.2027

Pseudobulbar affect

Author: Fardin Nabizadeh MD

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Editor: Victor W Mark MD

Pseudobulbar affect

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Introduction

Overview

Pathologic laughter and crying occur in several neurologic disorders. This article describes the anatomical location of various brain centers for laughter and crying as well as the pathophysiology. Differential diagnosis, diagnostic workup, and management are described. In patients with cerebrovascular disease, pathologic laughter and crying may be warning signals that require prompt investigation and treatment of the underlying pathology. Antidepressants have been found to be useful in the management of these disorders.

Key points

	• Pathologic laughter and crying are manifestations of neurologic disorders.
	• Disturbances at various levels of the central nervous system are involved, although lesions of the brainstem are associated with pathologic laughter and crying.
	• Neurologic investigations for these symptoms are aimed at detection of treatable lesions, eg, benign intracranial neoplasms.
	• Antidepressants, particularly serotonin reuptake inhibitors, are usually effective for the symptomatic management of pathologic crying and laughter.
	• Pathological laughter and crying are common and impair the quality of life, but treatment is available to manage these problems.

Historical note and terminology

Laughter has occupied philosophers from antiquity to modern times. It is generally associated with joy and humor. Laughter is elicited by a variety of stimuli and may be a reflex or a voluntary reaction to a certain situation or an expression of psychopathology. Pathologic laughter is defined as laughter that is inappropriate, uncontrolled, or dissociated from any stimulus. Pathologic laughter, often associated with crying, is also referred to as pseudobulbar affect and can occur as a part of emotional incontinence in neuropsychiatric disorders. Inappropriate laughter can occur in Witzelsucht and manifest as a tendency to tell inappropriate jokes or euphoric behavior due to focal right-orbitofrontal parenchymal lesions (77).

Less severe forms of the disorder following brain injury are often referred to as "emotionalism"; they are further specified as emotionalism-laughter or emotionalism-crying. Pathologic laughter or crying are included in the category of “involuntary emotional expression disorders” because they are disorders of emotional expression rather than affective mood disorders in which laughter and crying are associated with feelings of happiness or sadness. Episodes have been reported of spontaneous, uncontrollable laughter erupting from the congregations, even during times of solemn ceremony or messages from the pulpit. These episodes of "holy laughter" in charismatic Christian sects are not pathologic.

One of the oldest documented cases of pathologic laughter and crying is that by Ambroise Pare, the 16th-century French surgeon. He described women who wept and laughed without reason and did not respond to any treatment (28). A French physician, Trousseau, described pathologic laughter accompanying epileptic seizures (74). In 1886, cases of exaggerated emotional behavior, laughter as well as crying, were described in patients with lesions along the descending pathways to the brainstem termed “Zwangslachen und Zwangsweinen” in German (51).

Several isolated case reports in the literature over the past 20 years have described the association of pathologic laughter with a wide variety of neurologic disorders. The French refer to pathologic laughter preceding cerebrovascular ischemia as fou rire prodromique, which is translated as "prodrome of crazy laughter," and was first described by Charles Fere in 1903 (21). Although laughing and crying are lumped together, either of these may be the only manifestation. Fere reported pathologic laughter heralding an apoplectic event and was also among the first to describe gelastic epilepsy (25). Seizures accompanied by crying are referred to the rare condition “dacrystic seizures” first described by Zilgien in 1904 (82).

There has been considerable speculation in the past about the neural mechanisms of laughter. Wilson considered the mechanism to be in the region of the mesial thalamus, hypothalamus, and subthalamus (79). Papez hypothesized that supranuclear pathways, including those from the limbic system, mediate emotional expressions such as laughter and synapse in the reticular core of the brainstem (54). This fits in with a later postulate that the tegmentum near the periaqueductal gray matter contains the integrative mechanism for emotional expression (33). Pseudobulbar affect may be related to white matter degeneration, particularly in corticobulbar tracts (69).

Clinical manifestations

Presentation and course

	• Pathologic laughter and crying may have an acute or gradual onset in chronic neurologic disorders.
	• Episodes of laughter may alternate with crying spells and may rarely be the first or the sole manifestation.
	• The prognosis depends on the primary pathology.

Pathologic laughter or crying occurs out of context to the social setting, is usually unprovoked, and is not necessarily associated with the patient's underlying emotion. Pathologic laughter episodes resemble severe, spontaneous, nonpathologic laughter. Darwin's classical description of laughter is as follows:

During excessive laughter, the whole body is often thrown backwards and shaken, or almost as often, convulsed; respiration is much disturbed, the head and the face become engorged with blood, with the veins distended; the orbicularis muscles are spasmodically contracted...to protect the eyes. Tears are freely shed (16).

Pathologic laughter may have an acute or gradual onset in chronic neurologic disorders. It is usually a part of a set of neurologic and neurobehavioral manifestations but may rarely be the first or sometimes the sole manifestation. The episodes of laughter may alternate with crying spells. Usually there are no triggering factors, but occasionally, smiling at a patient with this disorder might precipitate a fit of laughter.

The duration of episodes of laughter is usually short (ie, less than a minute), but may last up to an hour or until the patient is exhausted. Accompaniments may include spasmodic skeletal muscle contractions or seizures. Following the cessation of laughing, there is a variable period during which the muscles remain flaccid. Occasionally, paralysis in stroke patients may be observed after the fit of laughing is over.

Prognosis and complications

The prognosis depends on the primary pathology. Most of the cases with benign lesions described in the literature can be managed successfully. There are no case reports of any spontaneous remissions of the condition. Pathologic laughter and crying are socially embarrassing and even frightening for patients and their caregivers, but they have few medical complications. Laughter can provoke catalepsy in patients with narcolepsy.

Clinical vignette

The following is an instructive case report. A 59-year-old right-handed man with a history of episodes of ischemic stroke in the territory of the left middle cerebral artery, which resulted in right hemiparesis and aphasia, presented with pathological laughter and crying (18). A differential diagnosis between gelastic seizures and episodes of pathological laughter as a manifestation of repeated ischemic attacks was made. MRI showed lacunar infarcts in the left lenticular-capsular-thalamic area. There was some atherosclerosis in the carotid arteries and mitral stenosis, but no cardiac source of thromboembolism was identified. Transient ischemic attacks continued despite anticoagulation. Eventually, the mitral valve was replaced resulting in cessation of ischemic attacks and relief from pathological laughter and crying.

Biological basis

	• Control of laughter may occur at the cortical or bulbar level with integration at the subthalamic level.
	• Expression of laughter depends on an involuntary system involving the amygdala and the brainstem, as well as a voluntary system originating in the frontal areas and leading through the motor cortex and pyramidal tract to the ventral brainstem.

Anatomic localization

The neuroanatomical localization of laughter is poorly defined. Control of laughter may occur at one or more of the following three levels: (1) a cortical level, probably the cingulate gyrus; (2) a bulbar or effector level; and (3) an integrative level, probably in the subthalamic. Lesions at any of these levels may produce pathologic laughter.

The medulla is the putative center for laughter and crying in the brainstem. Lesions in many areas of the brainstem cause abnormal emotional activity. The serotonergic raphe nuclei in the brainstem, which plays a role in the mechanism of pathologic crying, give rise to long projections to the limbic forebrain structures. The major ascending pathway from the rostral raphe nuclei joins the medial forebrain bundle in the lateral hypothalamus. Fibers leaving this main ascending bundle enter the substantia nigra, the intrathalamic nuclei, the stria terminalis, the septum, and the internal capsule.

Studies on volunteers during laughter show fMRI activity in the anterior supplemental motor area. Although the ventromedial frontal lobe is likely the center for perceiving what is funny, the accompanying laughter and feeling of mirth may be triggered by connections to other areas of the brain that are involved in control of movements of the mouth as well as positive emotions. Brain imaging with MRI shows pathological changes in the cerebellum, pons, pontocerebellar tracts, inferior olivary nuclei, and olivocerebellar tracts, but no degenerative changes are found in the corticobulbar or corticospinal tracts or in the serotoninergic raphe nuclei (78). A study revealed an augmented functional connectivity between the middle cerebellar peduncles and the posterior cingulate cortex, as well as a reduced functional connectivity between the middle cerebellar peduncles and the left middle frontal gyrus in patients with relative to patients without pseudobulbar affect. These findings suggest that certain distortions of the fronto-tempo-parietal-cerebellar circuits could be associated with the occurrence of pseudobulbar affect in amyotrophic lateral sclerosis. Notably, the anomalous functional connectivity between the cerebellum and the posterior cingulate cortex and the left middle frontal gyrus in pseudobulbar affect patients compared to those without pseudobulbar affect emphasizes the role of the cerebellum in regulating the expression of emotions in amyotrophic lateral sclerosis patients (73).

Acute stimulation of an electrode located in the subthalamic nucleus during treatment of Parkinson disease induces loud laughter if stimulation parameters are raised higher than therapeutic level. Deep cerebellar electrical stimulation during treatment of patients with cerebral palsy can produce episodes of laughter.

Expression of laughter depends on two partially independent neuronal pathways:

	(1) An “involuntary” or “emotionally driven” system, involving the amygdala, thalamic/hypo- and subthalamic areas, as well as the dorsal/tegmental brainstem.
	(2) A “voluntary” system, originating in the premotor/frontal opercular areas and leading through the motor cortex and pyramidal tract to the ventral brainstem.

These systems and the laughter response are coordinated by a center in the dorsal upper pons. Analysis of pontine lesions associated with pathological laughter and crying reported in the literature indicate a regulatory center in the pons with the most consistently involved region in the anterior paramedian pons, which may also be the site of a faciorespiratory center (19).

Pathophysiology

Pathologic laughter and crying are due to damage of pathways that arise in the motor areas of the cerebral cortex and descend to the brainstem to inhibit the center for laughter and crying. Based on this concept, laughter and crying would be considered "disinhibition" or "release" phenomena. Based on a case study, it has been proposed that the critical lesions in pathologic crying and laughter occur in the cerebro-ponto-cerebellar pathways (58). Therefore, the cerebellar structures that automatically adjust the execution of laughter or crying to the cognitive and situational context of a potential stimulus receive incomplete information. This results in inadequate and even chaotic behavior manifested as pathologic crying and laughter. Occurrence of pathologic laughter in cerebellar types of multiple system atrophy supports the view that cerebellum and its interconnected structures may be involved in the regulation of emotional expression.

Although pathologic laughter is mainly observed in various neurologic diseases in adults, rarely children may be affected. A 6-year-old child with acute cerebellitis after varicella presented with ataxia, dysmetria, mutism, and pathological laughter (13). Clinical-anatomic correlations performed in patients with focal infarcts in the basilar pons reveal that pathologic laughter results from rostral and medial pontine lesions and may result from disruption of the pontine component of associative corticopontocerebellar circuits. Increased pontine activation in pathologic laughter has been demonstrated with functional MRI but disappeared after successful treatment with paroxetine, a selective serotonin reuptake inhibitor (37).

Intraoperative electric cortical and subcortical stimulation mapping in an awake patient with diffuse astrocytoma of the right superior frontal gyrus and stimulation of the cingulum medially and inferiorly to the tumor elicited laughter without mirth (22). These findings support the role of the cingulum in the motor component of the mechanism, which is a useful functional landmark to identify the cingulum during subcortical mapping as a functional limit of the resection of intrinsic tumors.

Emotional incontinence manifested as episodes of crying and laughter are frequent in patients with small lenticulocapsular stroke. The findings appear to be consistent with the role of damage to serotonergic fibers in emotional incontinence, as they are particularly abundant in the internal globus pallidus.

A case of severe pathologic crying has been described after a limited left anterior choroidal artery territory infarction (17). This condition may be attributable to stroke-induced unilateral damage of the left capsular ascending projections of the serotonergic raphe nuclei. A single limited subcortical left-sided lesion with a critical topography regarding serotonergic pathways may cause permanent pathologic crying.

Furthermore, a case pseudobulbar affect was reported in an elderly woman with small vessel ischemic disease and alcohol abuse disorder (62). Thus, it is essential to recognize the possibility that pseudobulbar affect could occur in these disorders.

In cases of unilateral lesions, the left-sided lesions are more often associated with crying and the right-sided lesions with laughter. The cause of this dichotomy is not clear, but one explanation is that the left hemisphere's frontal lobes mediate emotions with a positive valence, and the right hemisphere mediates emotions with a negative valence.

In the circuitry involved in pathologic laughter and crying, ventral pons appears to be a crucial location, but further investigations are needed to determine how lesions in the basis pontis affect the activity of the cerebellum and the brainstem (57).

Causes of pathological laughing and crying can be classified in two groups (05):

	(1) Altered behavior with unmotivated happiness: Angelman syndrome, schizophrenia, manias, dementia, etc.
	(2) Interference with the inhibitory and excitatory mechanisms: gelastic epilepsy, fou rire prodromique in strokes, multiple sclerosis, amyotrophic lateral sclerosis, Parkinson disease, traumatic brain injury, brain tumors, etc.

Another concept is that lesions of the corticopontine projections can produce pathological laughing and crying whereas direct activation of the emotional pathway can result in emotional lability and the laughing or crying of gelastic epilepsy (39). A 2-hit model of pathological laughter and crying has been proposed, which is based on the analysis of lesion network-symptom-mapping: a combination of direct lesion and indirect diaschisis effects cause pathological laughter and crying through the loss of inhibitory cortical control of a dysfunctional emotional system (35).

A novel classification is based on pathogenesis as well as clinical and imaging findings of patients with disorders of laughter and crying. Patients are divided, according to intensity and frequency of laughter and crying, into hypoactive or hyperactive disorders of laughter and crying and subdivided into five subtypes: sensory (positive and negative), motor (positive and negative), and mixed (24). “Positive" and "negative" describe causation by irritative versus destructive lesions, respectively.

Pathophysiologically, pathological laughing and crying involves white matter degeneration, which can impair voluntary control over emotional expressions (69). Additionally, damage to the cortico-subcortical-thalamo-cerebellar circuitry and dysregulation of neurotransmitters like serotonin and norepinephrine further contribute to emotional dysregulation. This complex interplay of neural and chemical disruptions underscores the multifaceted nature of pathological laughing and crying and the need for targeted therapeutic approaches.

Pathological crying. This is devoid of any emotional counterpart, and crying spells known to occur due to various brainstem, cortical hemispheric, or cerebellar lesions or, quite rarely in "dacrystic" epilepsy. Following a mild left thalamic stroke, a patient presented with crying spells triggered by thumb-index rubbing of his right hand with no emotional counterpart (09). In this patient, loss of sensation seemed to generate crying spells rather than the more common allodynia. The authors speculate that the pathway providing inhibition from the lateral to the medial segment of the ventral postero-lateral thalamus, which is linked to the anterior cingulate (limbic) cortex engaged in emotional behavior, might have been selectively affected. Pathologic tearfulness is reported in 50% of cases of autoimmune limbic encephalitis with no neuropsychiatric manifestations and indicates abnormalities in networks of emotion regulation beyond the acute hippocampal focus (04).

Differential diagnosis

Disorders that are known to be associated with pathologic laughter and crying are shown in Table 1.

Table 1. Disorders Known to be Associated with Pathologic Laughter and Crying

• Angelman syndrome
• Central pontine myelinolysis
• Brain tumors
• Disseminated encephalomyelitis
• Drugs and toxins
• Dacrystic epilepsy
• Gelastic epilepsy
• Movement disorders
• Multiple sclerosis
• Neurodegenerative disorders: amyotrophic lateral sclerosis, Alzheimer disease, Parkinson disease, progressive supranuclear palsy, multiple system atrophy, Creutzfeldt-Jakob disease
• Neurosurgical procedures on basal ganglia
• Pseudobulbar palsy
• Psychiatric disorders
• Sleep-laughing (hypnogely)
• Stroke
• Traumatic brain injury
• Vascular malformations and aneurysms

Angelman syndrome. This is a genetic disorder that is associated with a deletion on chromosome 15 and is characterized by abnormalities or impairments in neurologic, motor, and intellectual functioning. Inappropriate and excessive laughter may occur in this syndrome.

Brain tumors. Tumors, mostly benign and occurring in a wide variety of locations, can manifest as pathologic laughter. Among the hemisphere tumors, those involving the frontal and temporal lobes are more likely to be associated with episodes of laughter.

Several case reports indicate that intrinsic as well as extrinsic tumors in the region of the brainstem are associated with pathologic laughter. Involuntary and inappropriate laughter may be an early sign of a meningiomas compressing ventrolateral brainstem and is relieved after resection of the tumors. Pathological laughter was one of the presenting symptoms of a giant clivus chordoma compression in the brainstem and was relieved following resection of the tumor by a transsphenoidal approach (27). Two cases of acoustic schwannoma presented with pathologic laughter that was resolved in each case by complete resection of the tumor (43). Cranial nerve tumors, arising in the cerebellopontine angle and compressing the brainstem, may produce similar effects. In several patients with trigeminal schwannoma who displayed symptoms of pathologic laughter and crying, there was no recurrence of laughter and crying attacks after total removal of the tumors. A patient who presented with pathologic crying caused by a trigeminal schwannoma was shown to have a tumor-associated cyst indenting the pons (11). Similarly, a patient with trochlear nerve neurinoma presented with pathologic laughter as the principal symptom, which was cured by tumor resection (44). Another case of trochlear nerve neurinoma presenting with pathological laughter and diplopia was reported, which resolved after excision of the tumor (63).

Pathologic laughter reported in children with pontine glioma is due to disruption of a network of cerebro-ponto-cerebellar pathways (29). Pathologic laughter and gelastic syncope have been reported as the sole presenting features of cerebellar ependyma (20). Hypothalamic hamartomas are frequently associated with gelastic and dacrystic seizures. A patient with a poorly differentiated metastatic pulmonary carcinoma in the pons presented with involuntary, persistent, and unmotivated laughter that preceded other clinical manifestations (61). A patient with glioblastoma multiforme in the right prefrontal area presented with pathologic laughter, which resolved after resection of the tumor (75). Well before other neurologic signs/symptoms, pathologic laughter may be the only symptom of a focal mass lesion causing ventrolateral upper brainstem compression such as petroclival meningioma (26).

Disseminated encephalomyelitis. Pseudobulbar affect due to acute disseminated encephalomyelitis is rare. According to a case report, a young Chinese woman manifested pseudobulbar affect due to disseminated encephalomyelitis for seven years (40). The patient's principal symptoms were extreme emotions or tears on hearing about sad news and uncontrollable laughter.

Drugs and toxins. Pathologic laughter can be a side effect of therapeutic drugs, drugs of abuse, or a manifestation of exposure to toxins. Inappropriate, uncontrollable laughter has been reported following intravenous sodium valproate for treatment of epilepsy. Pathologic laughter has been reported to be induced by sumatriptan (08). Uncontrollable laughter has been observed in healthy adults after marijuana intoxication in the absence of any pathologic changes in the brain. Inhalation of an insecticide was reported to induce pathologic laughing lasting 40 minutes, which was controlled by intravenous diazepam (81). Pathologic laughter has been reported in a patient with pontine hemorrhage following administration of atomoxetine as a cognitive enhancer (56). This resolved after discontinuation of atomoxetine. Atomoxetine is a CNS stimulant that increases norepinephrine and dopamine levels in the prefrontal cortex, which might play a role in the development of pathologic laughing.

Dacrystic epilepsy. This rare disorder is also referred to as "crying seizures" or “ictal weeping.” When dacrystic seizures are accompanied by gelastic seizures, the underlying lesion is a hypothalamic hamartoma, but when gelastic seizures are absent, the underlying etiology is of cortical (especially temporal) origin. Patients with dacrystic seizures generally have an underlying brain structural lesion, are frequently refractory to antiepileptic drugs, and often have a poor prognosis for seizure control (12).

Gelastic epilepsy. Laughter seizures are more likely to occur in epilepsies of frontal or temporal lobe origin. These may be associated with brain tumors or cerebral atrophy in these locations. Clinical features include absence of history of other conditions associated with pathologic laughter and presence of other manifestations generally accepted as epileptic. In an infant with intractable gelastic seizures, ictal positron emission tomography demonstrated epileptiform activity within a hypothalamic hamartoma (64). A teenager whose gelastic epilepsy due to an underlying hypothalamic hamartoma was found refractory to various antiepileptic drugs was treated successfully by stereotactic radiosurgery, resulting in total cessation of seizures (68).

Movement disorders. In a pilot study on patients admitted to a movement disorder clinic, 75.7% had pathologic crying, 13.5% had pathologic laughter, and 10.8% had both (66). The prevalence of both crying and laughter in individual diagnostic categories was 4.7% in idiopathic Parkinson disease, 2.7% in primary dystonia, and 3.1% in essential tremor.

Multiple sclerosis. Pathologic laughing and crying, which are distinct from emotional lability, occur in 10% of patients with multiple sclerosis. Severely disabled patients, generally with longstanding disease and cognitive deficits, are more likely to develop it. Pathologic laughing and crying in multiple sclerosis are likely due to involvement of the prefrontal cortex. There is no definite correlation with the location of cerebral lesions in demyelinating disorders. In a young woman presenting with acute pathologic laughter as a manifestation of demyelinating disease, MRI demonstrated lesions in the cerebral peduncles (48). A case has been reported of a patient who presented with paroxysmal hemidystonia along with bursts of pathologic laughter as the first manifestation of multiple sclerosis (01). There is a case report of pathologic laughter as the presenting symptom of clinically isolated brainstem syndrome due to a demyelinating process demonstrated by MRI and magnetic resonance spectroscopy (36).

Neurodegenerative disorders. Several neurodegenerative disorders are associated with pathologic crying and laughter. In one study of Alzheimer disease patients, 25% showed crying and 14% showed laughing or mixed (laughing and crying) episodes (67). Patients with mixed pathologic affect showed significantly more subcortical atrophy on CT than patients with pathologic affect crying. Pathologic laughing and crying seem to be more common in patients with amyotrophic lateral sclerosis than in patients with other neurodegenerative diseases (45). The findings of a study of behavioral physiology in these patients support the idea that pathological laughing and crying represents activation of all channels of emotional response, including behavioral, physiological, and subjective responses (50). Pathologic laughter occurs in 36% of patients with a cerebellar type of multiple system atrophy (58).

Pathological laughter and crying has been reported in three patients with Creutzfeldt-Jakob disease who had a mutation of prion protein gene codon180 (31). Widespread cerebral cortical involvement that is characteristic of this form of Creutzfeldt-Jakob disease was offered as an explanation of these symptoms.

Neurosurgical procedures on basal ganglia. History of neurosurgical procedures helps to identify the cause. Transient episodes of pathologic laughter occasionally follow deep brain stimulation. Emotional incontinence is included in the neurobehavioral complications of pallidotomy. A case has been reported of pathologic laughter after gamma knife thalamotomy, which resolved after treatment with sertraline (49). Pathologic crying has been reported following high-frequency deep brain stimulation in the region of the caudal internal capsule in a patient with Parkinson disease (41). Pathological crying has also been reported after subthalamic nucleus stimulation (55). A patient developed pathologic crying immediately postoperatively following deep brain stimulation of the subthalamic nucleus for Parkinson disease, and spread of the current to adjacent cortico-ponto-cerebellar pathways was considered to be responsible (80).

Pseudobulbar palsy. The term pseudobulbar palsy is used to describe uncontrolled activity of the lower motor neurons of the bulbar region and is a phenomenon that seems to cause laughing and crying not necessarily associated with emotions. The loss of the upper motor neurons also results in loss of control of these physical manifestations of emotion. A patient with pseudobulbar palsy presented with three episodes of spasmodic laughter, which had induced syncope (07).

Psychiatric disorders. Pathologic laughter and crying due to brain lesions are differentiated as emotional incontinence from lability of affect of mood disorders. However, when combined lesion of thalamic or brainstem structures and corticofugal motor projection systems are the pathoanatomic basis of affect incontinence, both affect lability and incontinence may be present. Pathologic laughter and crying may occur as manifestation of posttraumatic stress disorder. Pathologic laughter can present primarily as an obsessive-compulsive phenomenon. Inappropriate laughter has been reported in a patient with mental retardation and personality disorder (10).

Sleep-laughing (hypnogely). In most cases, hypnogely presents as a benign physiological phenomenon related to dreaming and REM sleep (72). Hypnogely is a symptom of neurologic disorders in only a minority of patients. It differs from physiological laughing as the sense of mirth is absent.

Stroke. Approximately one third of stroke patients develop emotional lability. Neuroradiological and neuropathologic studies of patients with pathologic laughter following cerebrovascular events have shown lesions in the internal capsule and thalamus, basal ganglion, hypothalamus, and ventral pons. Pathologic laughter may be the first manifestation of stroke. A transient fit of laughter can be the inaugural symptom of capsular-thalamic infarction. Prodromal pathologic laughter marked the onset of bilateral capsular genu infarction, demonstrated by MRI, in a patient (76). Pathological laughter has been reported as a manifestation of cerebral infarction due to middle cerebral artery occlusion. A patient with subarachnoid hemorrhage whose ruptured aneurysm was successfully obliterated surgically developed vasospasm resulting in cerebral infarction in the territory of middle cerebral artery and impaired consciousness (70). Pathological laughter developed six months after onset of initial ictus and when the patient had recovered consciousness, and it was successfully managed with sertraline. In another patient, sudden onset of left hemiparesis preceded by pathological laughter was overshadowed by severe behavioral changes, so that the diagnosis of stroke was missed until two days later when an MRI showed middle cerebral artery occlusion and the patient had passed the window for thrombolysis (52).

A case that presented with uncontrollable and unemotional laughter lasting an hour was followed by facial-brachial paresis due to pontine ischemia caused by vertebrobasilar stenosis, which progressed to bilateral brainstem infarction and resulted in death (23). A similar case of brainstem ischemia had a more favorable outcome after thrombolysis (15). Basilar artery occlusion is also associated with pathologic crying as a prodromal symptom expressed in French as folles larmes prodromiques (38).

Traumatic brain injury. Patients with traumatic brain injury can develop a pseudobulbar palsy with uncontrollable laughter and crying. The prevalence of pathologic laughter and crying during the first year after traumatic brain injury was 10.9% and usually associated with the presence of anxiety disorder and frontal lobe lesions (71).

Vascular malformations. Large aneurysms of the middle cerebral artery can produce the space-occupying effect of tumors in the temporal lobe region and present with pathologic laughter. A case has been reported of angiographically occult brainstem vascular malformation presenting solely with pathologic laughing and crying, which resolved after occlusion of the malformation by proton beam therapy (06). There was no manifestation of pseudobulbar palsy in this case.

Confusing conditions

Pathologic laughter may resemble severe, spontaneous, normal laughter, but it occurs out of context to the social setting, is usually unprovoked, and is not necessarily associated with the patient's underlying emotion. As a deficit in regulation and coordination of emotional expression, pathologic laughter and crying differ from mood disorders, which are characterized by a pervasive and sustained problem of emotional experience.

Management

	• Removal of the cause by surgery, eg, a brain tumor.
	• Excision of the epileptogenic focus in patients with gelastic epilepsy.
	• Dextromethorphan-quinidine is approved for treatment of emotional lability.
	• Lamotrigine has been used successfully in the treatment of pathologic laughing and crying following traumatic brain injury and stroke.

The management of benign intracranial tumors associated with pathologic laughter and crying is surgical resection, which usually resolves the symptoms. In a patient who presented with pathologic laughter due to a large suprasellar cyst causing severe compression of the midbrain and pons, spontaneous laughing spells disappeared immediately after surgery (14).

A patient who suffered from epigastric psychic auras, complex partial seizures with a gelastic component, and secondarily generalized seizure with ictal involvement of the temporobasal region became seizure-free following right temporal lobe resection (47). Removal of the epileptogenic focus in patients with gelastic epilepsy of frontal lobe origin has been reported to result in good control of gelastic seizures (30).

In patients with cerebrovascular disease, pathologic laughter and crying may be the warning signals, which require prompt investigation and treatment of the underlying pathology. A review of placebo-controlled clinical trials in patients with stroke and emotionalism concluded that antidepressants may reduce the frequency and severity of crying or laughing episodes based on very low-quality evidence, and more reliable data are required before any definite recommendations can be made about the treatment of poststroke emotionalism (02).

In 2010, dextromethorphan-quinidine received approval from the U.S. Food and Drug Administration as first-in-class pharmacotherapy for emotional lability. Selective serotonin reuptake inhibitors (SSRIs) are the drugs of choice for pathologic crying after brain injury and accompanying depression. Potential benefits of SSRIs include treatment without using multiple drugs and the possibility of tailoring treatment to the individual patient (59). Frequently used preparations are fluoxetine, sertraline, citalopram, and paroxetine. Treatment with sertraline has been found to improve patients with pathologic crying and laughter without significant side effects. Citalopram and paroxetine are equally effective in the management of pathologic crying and laughter in patients with traumatic brain injury. The adverse effect after paroxetine is nausea and vomiting, whereas citalopram is usually well tolerated and without adverse effects. In randomized studies, citalopram has been shown to be effective in at least 50% of patients with pathologic crying. Citalopram has been used successfully for the treatment of pseudobulbar affect following progressive multifocal leukoencephalopathy (34). Furthermore, the use of escitalopram for pseudobulbar affect following severe traumatic brain injury was reported (03).

The rationale for the use of SSRIs is based on the evidence that serotonergic neurotransmission may be damaged in emotional incontinence.

If selective serotonin reuptake inhibitors are ineffective or not well-tolerated, second-line treatment options such as tricyclic antidepressants, noradrenergic reuptake inhibitors, dopaminergic agents, and uncompetitive N-methyl-D-aspartate receptor antagonists may be useful.

Significant and rapid recovery in both pathologic laughing and crying following stroke has been reported with lamotrigine treatment. Lamotrigine has been used successfully in the treatment of pathologic laughing and crying following traumatic brain injury. Duloxetine, a serotonin-norepinephrine reuptake inhibitor approved for the treatment of depression and neuropathic pain, is also useful for the treatment of pathologic laughter and crying. A prospective study showed that duloxetine could attenuate pathologic laughing exhibited by stroke patients, but randomized controlled studies are required to validate these findings (65).

A 60-year-old woman with multiple sclerosis presented with unrelenting crying as a manifestation pseudobulbar affect or emotional incontinence and was already unresponsive to SSRIs and dextromethorphan/quinidine but did respond to valproic acid (32).

Outcomes

Patients with benign lesions of the brain are relieved of pathological laughter in most cases. Those with damage to the brain, such as in stroke, have a variable degree of improvement and success in controlling symptoms by medications.

References

01: Aguirregomozcorta M, Ramió-Torrentà L, Gich J, Quiles A, Genís D. Paroxysmal dystonia and pathological laughter as a first manifestation of multiple sclerosis. Mult Scler 2008;14(2):262-5. PMID 17942514
02: Allida S, Patel K, House A, Hackett ML. Pharmaceutical interventions for emotionalism after stroke. Cochrane Database Syst Rev 2019;3:CD003690.** PMID 30887498
03: Amir Malik MF, Jafri MAK, Nizami AT. Use of Escitalopram for pseudobulbar affect following severe traumatic. J Pak Med Assoc 2023;73(2):416-8. PMID 36800742
04: Argyropoulos GPD, Moore L, Loane C, et al. Pathologic tearfulness after limbic encephalitis: a novel disorder and its neural basis. Neurology 2020;94(12):e1320-35.** PMID 31980582
05: Arias M. Neurology of laughter and humour: pathological laughing and crying. [Spanish] Rev Neurol 2011;53(7):415-21. PMID 21948012
06: Asfora WT, DeSalles AA, Abe M, Kjellberg RN. Is the syndrome of pathological laughing and crying a manifestation of pseudobulbar palsy. J Neurol Neurosurg Psychiatry 1989;52:523-5. PMID 2738597
07: Awada A, Halaby G, Tamraz J. Spasmodic laughter syncope. An unusual complication of pseudobulbar palsy. Rev Neurol (Paris) 2009;165(1):86-8. PMID 18808775
08: Barbanti P, Fabbrini G, Berardelli A. Acute pathological laughter induced by sumatriptan. Cephalalgia 2008;28(1):92-3. PMID 17868284
09: Bassani R, Rosazza C, Ghirardin L, et al. Crying spells triggered by thumb-index rubbing after thalamic stroke: a case report. BMC Res Notes 2017;10(1):109. PMID 28235422
10: Beke DB, Hebbrecht M. Pathological laughter. A case study. Tijdschr Psychiatr 2007;49(5):333-7. PMID 17492584
11: Bhaskar IP, Chacko AG, Daniel RT. Brainstem compression from a trigeminal schwannoma presenting with pathological crying. J Clin Neurosci 2008;15(3):322-4. PMID 18191401
12: Blumberg J, Fernández IS, Vendrame M, et al. Dacrystic seizures: demographic, semiologic, and etiologic insights from a multicenter study in long-term video-EEG monitoring units. Epilepsia 2012;53(10):1810-9. PMID 22780551
13: Brito T, Oliveira I, Silva L, Parente S. Transient mutism, pathological laughter and cerebellar ataxia after primary varicella-zoster virus infection. BMJ Case Rep 2019;12(11):e230683. PMID 31704797
14: Cao Z, Lv J, Ding Z, Du H. Pathological laughter in a patient with Rathke cleft cyst. J Clin Neurosci 2008;15(11):1279-82. PMID 18771927
15: Couderq C, Drouineau J, Rosier MP, Alvarez A, Gil R, Neau JP. Pathological laughter after the brainstem infarction. Rev Neurol (Paris) 2000;156:281-4. PMID 10740101
16: Darwin C. Expression of the emotions in man and animal. 2nd ed. New York: Appleton & Co, 1890.
17: Derex L, Ostrowsky K, Nighoghossian N, Trouillas P. Severe pathological crying after left anterior choroidal artery infarct. Reversibility with paroxetine treatment. Stroke 1997;28(7):1464-6. PMID 9227702
18: Dulamea AO, Matei C, Mindruta I, Ionescu V. Pathological laughter as prodromal manifestation of transient ischemic attacks--case report and brief review. BMC Neurol 2015;15:196. PMID 26459199
19: Elyas AE, Bulters DO, Sparrow OC. Pathological laughter and crying in patients with pontine lesions. J Neurosurg Pediatr 2011;8(6):544-7. PMID 22132910
20: Famularo G, Corsi FM, Minisola G, De Simone C, Nicotra GC. Cerebellar tumour presenting with pathological laughter and gelastic syncope. Eur J Neurol 2007;14(8):940-3. PMID 17662020
21: Fere MC. Le fou rire prodromique. Rev Neurol (Paris) 1903;7:353-8.
22: Fernández L, Santos C, Gómez E, Velásquez C, Martino J. Eliciting smiles and laughter during intraoperative electric stimulation of the cingulum: surgical scenario. World Neurosurg 2020;133:55.** PMID 31562962
23: Gondim FA, Parks BJ, Cruz-Flores S. "Fou rire prodromique" as the presentation of pontine ischaemia secondary to vertebrobasilar stenosis. J Neurol Neurosurg Psychiatry 2001;71(6):802-4. PMID 11723208
24: Gondim FA, Thomas FP, Cruz-Flores S, Nasrallah HA, Selhorst JB. Pathological laughter and crying: a case series and proposal for a new classification. Ann Clin Psychiatry 2016;28(1):11-21. PMID 26855981
25: Gondim FA, Thomas FP, Oliveira GR, Cruz-Flores S. Fou rire prodromique and history of pathological laughter in the XIXth and XXth centuries. Rev Neurol (Paris) 2004;160(3):277-83. PMID 15037840
26: Gosal JS, Pandey S, Das KK, et al. Pathologic laughter as an early and unusual presenting symptom of petroclival meningioma: a case report and review of the literature. World Neurosurg 2019;123:161-4. PMID 30554003
27: Gripp DA, do Souto AA, Gonsales D, et al. Giant clival chordoma causing pathological laughter. Surg Neurol Int 2014;5:18. PMID 24778906
28: Hamby WB. The case reports and autopsy records of Ambroise Pare. Springfield: Charles C. Thomas, 1960:6-7.
29: Hargrave DR, Mabbott DJ, Bouffet E. Pathological laughter and behavioural change in childhood pontine glioma. J Neurooncol 2006;77(3):267-71. PMID 16314950
30: Hu WH, Zhang K, Shao XQ, et al. Surgical outcome of gelastic epilepsy of frontal lobe origin: a case report. Seizure 2011;20(4):352-6. PMID 21208813
31: Iwasaki Y. Three cases of Creutzfeldt-Jakob disease with prion protein gene codon180 mutation presenting with pathological laughing and crying. J Neurol Sci 2012;319(1-2):47-50. PMID 22658899
32: Johnson B, Nichols S. Crying and suicidal, but not depressed. Pseudobulbar affect in multiple sclerosis successfully treated with valproic acid: case report and literature review. Palliat Support Care 2015;13(6):1797-801. PMID 24916672
33: Kelly AH, Beaton LE, Magoun HW. Midbrain mechanism for faciovocal activity. J Neurophysiol 1946;9:181-9. PMID 21028161
34: King RR, Reiss JP. Treatment of pseudobulbar affect with citalopram in a patient with progressive multifocal leukoencephalopthy. J Clin Neurosci 2012;19(1):185-6. PMID 22055296
35: Klingbeil J, Wawrzyniak M, Stockert A, et al. Pathological laughter and crying: insights from lesion network-symptom-mapping. Brain 2021;awab224.** PMID 34142117
36: Kocer B, Oner Y, Batur H, Nazliel B, Cengiz B, Tali T. Pathological laughing as a manifestation in a clinically isolated brainstem syndrome: a case report. J Neuroimaging 2009;19(3):291-4. PMID 18826440
37: Kosaka H, Omata N, Omori M, et al. Abnormal pontine activation in pathological laughing as shown by functional magnetic resonance imaging. J Neurol Neurosurg Psychiatry 2006;77(12):1376-80. PMID 17110751
38: Larner AJ. Basilar artery occlusion associated with pathological crying: 'folles larmes prodromiques'. Neurology 1998;51:916-7. PMID 9748065
39: Lauterbach EC, Cummings JL, Kuppuswamy PS. Toward a more precise, clinically-informed pathophysiology of pathological laughing and crying. Neurosci Biobehav Rev 2013;pii:S0149-7634(13)00062-6. PMID 23518269
40: Li Z, Luo S, Ou J, Huang R, Wang Y. Persistent pseudobulbar affect secondary to acute disseminated encephalomyelitis. Socioaffect Neurosci Psychol 2015;5:26210. PMID 25792370
41: Low HL, Sayer FT, Honey CR. Pathological crying caused by high-frequency stimulation in the region of the caudal internal capsule. Arch Neurol 2008;65(2):264-6. PMID 18268198
42: Moore SR, Gresham LS, Bromberg MB, et al. A self report measure of affective lability. J Neurol Neurosurg Psychiatry 1997;63:89-93. PMID 9221973
43: Muzumdar DP, Goel A. Pathological laughter as a presenting symptom of acoustic schwannoma: report of two cases. J Clin Neurosci 2003;10(3):384-6. PMID 12763354
44: Nadkarni TD, Goel A. Trochlear nerve neurinoma presenting as pathological laughter. Br J Neurosurg 1999;13:212-3. PMID 10616595
45: Nabizadeh F, Nikfarjam M, Azami M, Sharifkazemi H, Sodeifian F. Pseudobulbar affect in neurodegenerative diseases: a systematic review and meta-analysis. J Clin Neurosci 2022;100:100-7. PMID 35436682
46: Newsom-Davis IC, Abrahams S, Goldstein LH, Leigh PN. The emotional lability questionnaire: a new measure of emotional lability in amyotrophic lateral sclerosis. J Neurol Sci 1999;169:22-5. PMID 10540003
47: Oehl B, Biethahn S, Schulze-Bonhage A. Mirthful gelastic seizures with ictal involvement of temporobasal regions. Epileptic Disord 2009;11(1):82-6. PMID 19299231
48: Okuda DT, Chyung AS, Chin CT, Waubant E. Acute pathological laughter. Mov Disord 2005. PMID 16007658
49: Okun MS, Heilman KM, Vitek JL. Treatment of pseudobulbar laughter after gamma knife thalamotomy. Mov Disord 2002;17:622-4. PMID 12112225
50: Olney NT, Goodkind MS, Lomen-Hoerth C, et al. Behaviour, physiology and experience of pathological laughing and crying in amyotrophic lateral sclerosis. Brain 2011;134(Pt 12):3458-69. PMID 22155983
51: Oppenheim H, Siemerling E. Mitteilungen über pseudobulbärparalyse und akute bulbärparalyse. Berl Kli Woch 1886;46:791-4.
52: Ozel G, Maltête D, Lefaucheur R. Pathological laughter as a symptom of middle cerebral artery stroke. J Emerg Med 2018;55(5):707-9. PMID 30249344
53: Panitch HS, Thisted RA, Smith RA, et al. Randomized, controlled trial of dextromethorphan/quinidine for pseudobulbar affect in multiple sclerosis. Ann Neurol 2006;59(5):780-7. PMID 16634036
54: Papez JW. A proposed mechanism of emotions. Arch Neurol Psychiatr 1937;38:725-42. PMID 7711480
55: Pariwatcharakul P, Clough C, Shotbolt P, et al. Pathological crying after subthalamic nucleus stimulation. Mov Disord 2013;28(10):1348-9. PMID 23868460
56: Park JM, Kim YW, Choi S. Atomoxetine (strattera)-induced pathologic laughing in a patient with pontine hemorrhage: a case report. Clin Neuropharmacol 2021;44(2):77-9.** PMID 33480614
57: Parvizi J, Coburn KL, Shillcutt SD, Coffey CE, Lauterbach EC, Mendez MF. Neuroanatomy of pathological laughing and crying: a report of the American Neuropsychiatric Association Committee on Research. J Neuropsychiatry Clin Neurosci 2009;21(1):75-87. PMID 19359455
58: Parvizi J, Joseph J, Press DZ, Schmahmann JD. Pathological laughter and crying in patients with multiple system atrophy-cerebellar type. Mov Disord 2007;22(6):798-803. PMID 17290465
59: Pioro EP. Current concepts in the pharmacotherapy of pseudobulbar affect. Drugs 2011;71(9):1193-207. PMID 21711063
60: Robinson RG, Parikh RM, Lipsey JR, et al. Pathological laughter and crying following stroke: validation of a measurement scale and double-blind treatment study. Am J Psychiatry 1993;150:286-293. PMID 8422080
61: Rodriguez Campello A, Pascual Calvet J, Pou Serradell A. Crazy laughter: first manifestation of a pontine tumour. Neurologia 2003;18(4):225-8. PMID 12721870
62: Safari T, Dehbozorgi M, Laurent B. Pseudobulbar affect in an elderly female with small vessel ischemic disease and alcohol abuse disorder: a case report. Cureus 2024;16(5):e60472. PMID 38764710
63: Sasaki N, Matsuda A, Kanou K, Oka N, Kokuzawa J, Kaku Y. A case of trochlear nerve neurinoma presenting with pathological laughter. No Shinkei Geka 2020;48(10):909-13. [Article in Japanese] PMID 33071226
64: Shahar E, Goldsher D, Genizi J, Ravid S, Keidar Z. Intractable gelastic seizures during infancy: ictal positron emission tomography (PET) demonstrating epileptiform activity within the hypothalamic hamartoma. J Child Neurol 2008;23(2):235-9. PMID 18160558
65: Shin SH, Kim YW, Kim NY. Treatment of poststroke pathologic laughing with duloxetine: a case series. Clin Neuropharmacol 2019;42(2):60-3. PMID 30724786
66: Siddiqui MS, Fernandez HH, Garvan CW, et al. Inappropriate crying and laughing in Parkinson disease and movement disorders. World J Biol Psychiatry 2008;10:1-7. PMID 18609421
67: Starkstein SE, Migliorelli R, Teson A, et al. Prevalence and clinical correlates of pathological affective display in Alzheimer's disease. J Neurol Neurosurg Psychiatry 1995;59:55-60. PMID 7608711
68: Susheela SP, Revannasiddaiah S, Mallarajapatna GJ, Basavalingaiah A. Robotic-arm stereotactic radiosurgery as a definitive treatment for gelastic epilepsy associated with hypothalamic hamartoma. BMJ Case Rep 2013;2013. PMID 24027254
69: Tahedl M, Tan EL, Siah WF, et al. Radiological correlates of pseudobulbar affect: Corticobulbar and cerebellar components in primary lateral sclerosis. J Neurol Sci 2023;451:120726. PMID 37421883
70: Takeuchi H, Iwamoto K, Mukai M, Fujita T, Tsujino H, Iwamoto Y. Effective use of sertraline for pathological laughing after severe vasospasm due to aneurysmal subarachnoid hemorrhage: case report. Neurol Med Chir (Tokyo) 2014;54(3):231-5. PMID 24201096
71: Tateno A, Jorge RE, Robinson RG. Pathological laughing and crying following traumatic brain injury. J Neuropsychiatry Clin Neurosci 2004;16(4):426-34. PMID 15616168
72: Trajanovic NN, Shapiro CM, Milovanovic S. Sleep-laughing--hypnogely. Can J Neurol Sci 2013;40(4):536-9. PMID 23786736
73: Trojsi F, Di Nardo F, D'Alvano G, et al. Resting state fMRI analysis of pseudobulbar affect in Amyotrophic Lateral Sclerosis (ALS): motor dysfunction of emotional expression. Brain Imaging Behav 2023;17(1):77-89. PMID 36370302
74: Trousseau A. De L'Epilepsie. Clinique Medicale de L'Hotel-Dieu de Paris 1877:89-155.
75: Tsutsumi S, Yasumoto Y, Ito M. Pathological laughter caused by frontal glioblastoma: case report. Neurol Med Chir (Tokyo) 2008;48(7):307-10. PMID 18654050
76: Uzunca I, Utku U, Asil T, Celik Y. "Fou rire prodromique" associated with simultaneous bilateral capsular genu infarction. J Clin Neurosci 2005;12(2):174-5. PMID 15749423
77: Vardi J, Finkelstein Y, Zlotogorski Z, Hod I. L'homme qui rit: inappropriate laughter and release phenomena of the frontal subdominant lobe. Behav Med 1994;20(1):44-6. PMID 7919634
78: Walusinski O. Pathological yawning, laughing and crying. Front Neurol Neurosci 2018;41:40-9. PMID 29145182
79: Wilson SA. Pathological laughing and crying. J Neurol Psychopathol 1924;4:299-333. PMID 19983327
80: Wolf ME, Abdallat M, Blahak C, Krauss JK. Pathological crying induced by deep brain stimulation of the subthalamic nucleus in Parkinson's disease. J Clin Neurosci 2017;45:159-61.** PMID 28887071
81: Zellers GL, Frank M, Dougherty J. Pathological laughter. Ann Emerg Med 1990;19:327-9. PMID 2310073
82: Zilgien H. Rire et pleure spasmodique. Rev Medical (Nancy) 1906;38:1.12.

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Pseudobulbar affect

Differential Diagnosis

Angelman syndrome
brain tumors
drugs and toxins
gelastic epilepsy
multiple sclerosis
- neurodegenerative disorders
- pseudobulbar palsy
- psychiatric disorders
- sleep-laughing (hypnogely)
- stroke
- traumatic brain injury
- vascular malformations and aneurysms

	• Drug screen
	• Brain imaging
	• EEG and EMG
	• Neuropsychological assessment
	• Pathological laughter and crying scale

Pseudobulbar affect …

Pseudobulbar affect

Introduction

Overview

Key points

Historical note and terminology

Clinical manifestations

Presentation and course

Prognosis and complications

Clinical vignette

Biological basis

Anatomic localization

Pathophysiology

Differential diagnosis

Table 1. Disorders Known to be Associated with Pathologic Laughter and Crying

Confusing conditions

Diagnostic workup

Management

Outcomes

References

Contributors

Author

Editor

Former Authors

Patient Profile

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to access the full version.

Questions or Comment?

Also in This Category

Brain death/death by neurologic criteria

Hepatic encephalopathy

Bowel dysfunction in neurologic disorders

Coma due to primary brainstem and diencephalic lesions

Transient visual loss

Neuroimaging in acute stroke

Sports activities: neurologic complications

Neurotechnology: brain-computer and brain-machine interfaces

Pseudobulbar affect

Introduction

Overview

Key points

Historical note and terminology

Clinical manifestations

Presentation and course

Prognosis and complications

Clinical vignette

Biological basis

Anatomic localization

Pathophysiology

Differential diagnosis

Table 1. Disorders Known to be Associated with Pathologic Laughter and Crying

Confusing conditions

Diagnostic workup

Management

Outcomes

References

Contributors

Author

Editor

Former Authors

Patient Profile

This is an article preview. Start a Free Account to access the full version.

Questions or Comment?

Also in This Category

Brain death/death by neurologic criteria

Hepatic encephalopathy

Bowel dysfunction in neurologic disorders

Coma due to primary brainstem and diencephalic lesions

Transient visual loss

Neuroimaging in acute stroke

Sports activities: neurologic complications

Neurotechnology: brain-computer and brain-machine interfaces

This is an article preview.
Start a Free Account
to access the full version.