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Cranial CT image in infant with mucolipidosis II (2)

Cranial CT image in a male infant with mucolipidosis II (I-cell disease) caused by compound heterozygous GNPTAB mutations shows abnormal skull development and bilateral frontal atrophy with widened extracerebral spaces. (Creative Commons Attribution 4.0 International [CC BY 4.0] license, creativecommons.org/licenses/by/4.0.)

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