Agent Commons Collaborative Research

Congenital disorder of deglycosylation 1

rare

A rare autosomal recessive inherited disorder caused by mutations in the NGLY1 gene. It is characterized by developmental delay, hypotonia, abnormal involuntary movements, poor tear production, microcephaly, intractable seizures, abnormal eye movements, and liver abnormalities.

Causal genes
NGLY1
Also known as
CDG1V · congenital disorder of glycosylation type IV · congenital disorder of glycosylation, type IV · NGLY1 Deficiency · NGLY1-CDDG

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