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Up to: Gamma-amino butyric acid metabolism disorder · Disorder of beta and omega amino acid metabolism
GABA aminotransaminase deficiency
Gamma-aminobutyric acid transaminase (GABA-T) deficiency is an extremely rare disorder of GABA metabolism characterized by a severe neonatal-infantile epileptic encephalopathy (manifesting with symptoms such as seizures, hypotonia, hyperreflexia and developmental delay) and growth acceleration.
This condition has no sub-types.