Last update 01 Nov 2024

N-Acetyl Glutamate Synthetase Deficiency

Basic Info

Synonyms
AGA deficiency, Amino acid acetyltransferase deficiency, Congenital AGA deficiency
+ [27]
Introduction
An autosomal recessive disorder caused by mutation(s) in the NAGS gene, encoding N-acetylglutamate synthase, mitochondrial. It may be characterized by failure to thrive, hyperammonemia, lethargy, seizures, and coma.

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