PHGDH deficiency

3-Phosphoglycerate dehydrogenase deficiency (3-PGDH deficiency) is an autosomal recessive form of serine deficiency syndrome 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

Also known as: PHGDH deficiency, PHOSPHOGLYCERATE dehydrogenase deficiency, 3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form, PHGDHD

0 clinical trials for this condition and its sub-types, 0 tagged with PHGDH deficiency itself.