Sign Up for a Free Account

This is an image preview.
Start a Free Account
to view the full image.

Sign Up for a Free Account For information on discounts, see Plans & Pricing

  • Nearly 3,000 illustrations, including video clips of neurologic disorders.

  • Every article is reviewed by our esteemed Editorial Board for accuracy and currency.

  • Full spectrum of neurology in 1,200 comprehensive articles.

  • Listen to MedLink on the go with Audio versions of each article.

Muscle biopsy in centronuclear myopathy (2)

Type 1 fiber predominance is one of the histochemical abnormalities associated with centronuclear myopathy. Most fibers exhibiting central nuclei are atrophic and are histochemically type1. ATP-ase, pH 4.6. (Contributed by Dr. Andrew Waclawik.)

Related Article

Related Media

Associated Disorders

  • Becker muscular dystrophy
  • CIDP
  • Charcot-Marie-Tooth disease
  • Duchenne muscular dystrophy
  • Kearns-Sayre syndrome
  • Kugelberg-Welander disease
  • MELAS
  • MERRF
  • McArdle disease
  • Miyoshi distal myopathy
  • NARP
  • Nonaka distal myopathy
  • Stormorken syndrome
  • Welander distal myopathy
  • Werdnig-Hoffman disease
  • acid maltase deficiency
  • amyloidosis
  • carnitine palmitoyltransferase deficiency
  • central core disease
  • centronuclear myopathy
  • congenital fiber-type disproportion
  • cysticercosis
  • denervation atrophy
  • dermatomyositis
  • facioscapulohumeral muscular dystrophy
  • hereditary neuropathy with pressure palsy
  • inclusion-body myositis
  • leprous neuropathy
  • limb-girdle muscular dystrophy
  • myotubular myopathy
  • nemaline rod myopathy
  • peripheral nerve vasculitis
  • polymyositis
  • progressive external ophthalmoplegia
  • sarcoid myopathy
  • sarcoid neuropathy
  • spinal muscular atrophy
  • toxoplasmosis
  • trichinellosis
  • tubular aggregates myopathy