Variants
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COG4-CDG

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Description

COG4-CDG is an extremely rare form of CDG syndrome (see this term) characterized clinically in the single reported case to date by seizures, some dysmorphic features, axial hyponia, slight peripheral hypertonia and hyperreflexia.

ORDO

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

62

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Genes

External Links

  • OMIM

    613489

  • Orphanet

    263501

  • HPO
  • Medgen

    C3150736

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