Mucolipidosis III Gamma

Alternative Names

  • Ml III Gamma
  • Mucolipidosis III, Complementation Group C
  • Mucolipidosis IIIc
  • Ml IIIc
  • Mucolipidosis III, Iranian Variant Form
  • Mucolipidosis III, Variant Form
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WHO-ICD-10 version:2010

Endocrine, nutritional and metabolic diseases

Metabolic disorders

OMIM Number

252605

Mode of Inheritance

Autosomal recessive

Gene Map Locus

16p13.3

Description

Mucolipidosis type III gamma is an autosomal recessive disorder characterized clinically by short stature, skeletal abnormalities, cardiomegaly, and developmental delay. The disorder is caused by a defect in proper lysosomal enzyme phosphorylation and localization, which results in accumulation of lysosomal substrates. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
252605.G.1United Arab EmiratesYesNM_032520.5:c.499dupHomozygousAutosomal, RecessiveAl-Jasmi et al. 2013 5 siblings with mild...
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