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Results 1 - 5 of 5 for Acute hyperammonemia
  1. N-acetylglutamate synthase deficiency 
    ... in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia. Hum Genet. 2003 Apr;112(4):364-8. ...
    https://medlineplus.gov/.../n-acetylglutamate-synthase-deficiency - Genetics
  2. NAGS gene 
    ... in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia. Hum Genet. 2003 Apr;112(4):364-8. ...
    https://medlineplus.gov/genetics/gene/nags - Genetics
  3. Carbonic anhydrase VA deficiency 
    ... crisis) and brain function is abnormal (known as acute encephalopathy). ... the blood (hyperammonemia), problems with acid-base balance in the blood ( ...
    https://medlineplus.gov/.../carbonic-anhydrase-va-deficiency - Genetics
  4. CPT1A gene 
    ... develop in women during pregnancy. This disorder, called acute fatty liver ... (hyperammonemia), and abnormalities in liver enzymes. A small percentage ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
  5. Dihydrolipoamide dehydrogenase deficiency 
    ... this condition include excess ammonia in the blood (hyperammonemia), a buildup of molecules called ketones in the ... dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome. Mol Genet ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics