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

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

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↑ Gamma-amino butyric acid metabolism disorder (1) ↑ Disorder of beta and omega amino acid metabolism (0)

Including sub-types (0) Tagged with GABA aminotransaminase deficiency (0)

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