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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. CPT1A gene 
    ... can rapidly progress to liver failure. Signs of acute fatty liver of pregnancy include an abnormal accumulation of fat in the liver, hypoglycemia, increased levels of ammonia in the blood (hyperammonemia), and abnormalities in liver enzymes. A small percentage ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
  4. 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
  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