GABA aminotransaminase deficiency

MONDO:0013166

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.

Also known as: GABA aminotransferase deficiency, GABA transaminase deficiency, gamma-aminobutyric acid transaminase deficiency, 4 alpha aminobutyrate transaminase deficiency, ABAT, GABA-transaminase deficiency, GABAT, gamma aminobutyrate transaminase deficiency

24 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by