52 top medical experts on Gamma aminobutyric acid transaminase deficiency across 4 countries and 3 U.S. states, including 5 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Gamma aminobutyric acid transaminase 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.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: 4 alpha aminobutyrate transaminase deficiency,  GABA transaminase deficiency,  Gaba-Transaminase Deficiency,  Gamma aminobutyrate transaminase deficiency


  

        

                    


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