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Results 21 - 30 of 42 for AMMONIA OR BENZALKONIUM OR LIDOCAINE OR ASPIRIN
  1. Gyrate atrophy of the choroid and retina 
    ... disorder. Occasionally, newborns with gyrate atrophy develop excess ammonia in the blood (hyperammonemia), which may lead to ... which processes excess nitrogen (in the form of ammonia) that is generated when protein is broken down ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  2. CA5A gene 
    ... excess nitrogen and prevents it from accumulating as ammonia, a substance that is toxic to the brain. ... anhydrases VA and VB implicates both enzymes in ammonia detoxification and glucose metabolism. Proc Natl Acad Sci ...
    https://medlineplus.gov/genetics/gene/ca5a - Genetics
  3. Carbonic anhydrase VA deficiency 
    ... people with carbonic anhydrase VA deficiency have excess ammonia in the blood (hyperammonemia), problems with acid-base ... anhydrases VA and VB implicates both enzymes in ammonia detoxification and glucose metabolism. Proc Natl Acad Sci ...
    https://medlineplus.gov/.../carbonic-anhydrase-va-deficiency - Genetics
  4. Pyruvate carboxylase deficiency 
    ... infants have severe lactic acidosis, a buildup of ammonia in the blood (hyperammonemia), and liver failure. They ... carboxylase allows compounds such as lactic acid and ammonia to build up and damage organs and tissues. ...
    https://medlineplus.gov/.../pyruvate-carboxylase-deficiency - Genetics
  5. CPT1A gene 
    ... fat in the liver, hypoglycemia, increased levels of ammonia in the blood (hyperammonemia), and abnormalities in liver ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
  6. Mitochondrial complex V deficiency 
    ... vomiting, weakness, and rapid breathing. High levels of ammonia in the blood (hyperammonemia) can also occur in ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  7. PC gene 
    ... loss of pyruvate carboxylase allows lactic acid and ammonia, among other compounds, to build up and damage ...
    https://medlineplus.gov/genetics/gene/pc - Genetics
  8. Very long-chain acyl-CoA dehydrogenase deficiency 
    ... of Reye syndrome occur in children who take aspirin during these viral infections. VLCAD deficiency is estimated ...
    https://medlineplus.gov/...g-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  9. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 
    ... Reye syndrome are associated with the use of aspirin during these viral infections. HMG-CoA lyase deficiency ...
    https://medlineplus.gov/...oxy-3-methylglutaryl-coa-lyase-deficiency - Genetics
  10. Systemic mastocytosis 
    ... stress. Certain medications can also be triggers, including aspirin, opioids, or non-steroidal anti-inflammatory drugs (NSAIDs). ...
    https://medlineplus.gov/genetics/condition/systemic-mastocytosis - Genetics
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