Orphanet: SLC35A2 CDG
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SLC35A2-CDG

Disease definition

A rare, congenital disorder of glycosylation characterized by severe or profound global developmental delay, early epileptic encephalopathy, muscular hypotonia, dysmorphic features (coarse facies, thick eyebrows, broad nasal bridge, thick lips, inverted nipples), variable ocular defects and brain morphological abnormalities on brain MRI (cerebral atrophy, thin corpus callosum).

ORPHA:356961

Classification level: Disorder
  • Synonym(s):
    • CDG syndrome type IIm
    • CDG-IIm
    • CDG2M
    • Congenital disorder of glycosylation type 2m
    • Congenital disorder of glycosylation type IIm
  • Prevalence: <1 / 1 000 000
  • Inheritance: Unknown 
  • Age of onset: Infancy, Neonatal
  • ICD-10: E77.8
  • OMIM: 300896
  • UMLS: -
  • MeSH: -
  • GARD: 12403
  • MedDRA: -

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