3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form

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Name:
3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form
Description:
3-Phosphoglycerate dehydrogenase deficiency (3-PGDH deficiency) is an autosomal recessive form of serine deficiency syndrome (see this term) characterized clinically in the few reported cases by congenital microcephaly, psychomotor retardation and intractable seizures in the infantile form and by absence seizures, moderate developmental delay and behavioral disorders in the juvenile form
ORPHAcode:
79351
Synonyms:
PHGDH deficiency, infantile/juvenile form
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14