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Results 1 - 10 of 19 for AMMONIA OR ASPIRIN OR BACITRACIN OR BENZALKONIUM OR LIDOCAINE OR NEOMYCIN OR POLYMYXIN B OR WATER
  1. Carbamoyl phosphate synthetase I deficiency 
    ... 2004;27(6):787-8. doi: 10.1023/b:boli.0000045842.59768.ea. Citation on PubMed
    https://medlineplus.gov/...rbamoyl-phosphate-synthetase-i-deficiency - Genetics
  2. Argininosuccinic aciduria 
    ... 10.1023/a:1010560704092. Citation on PubMed Wilcken B, Smith A, Brown DA. Urine screening for ... Citation on PubMed
    https://medlineplus.gov/genetics/condition/argininosuccinic-aciduria - Genetics
  3. Ornithine translocase deficiency 
    ... translocase deficiency is an inherited disorder that causes ammonia and other substances to build up (accumulate) in the blood. Ammonia, which is formed when proteins are broken down ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  4. Arginase deficiency 
    ... acid arginine (a building block of proteins) and ammonia to accumulate gradually in the blood. Ammonia, which is formed when proteins are broken down ... is especially sensitive to the effects of excess ammonia.Arginase deficiency usually becomes evident by about the ...
    https://medlineplus.gov/genetics/condition/arginase-deficiency - Genetics
  5. Pyruvate carboxylase deficiency 
    ... infancy or early childhood.Pyruvate carboxylase deficiency type B has ... buildup of ammonia in the blood (hyperammonemia), and liver failure. They ...
    https://medlineplus.gov/.../pyruvate-carboxylase-deficiency - Genetics
  6. N-acetylglutamate synthase deficiency 
    ... Pauli S, Guffon N, Vianey-Saban C, Wermuth B, Koch HG. Identification of novel mutations ... 2005 Feb 24. Citation on PubMed
    https://medlineplus.gov/.../n-acetylglutamate-synthase-deficiency - Genetics
  7. 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
  8. Systemic mastocytosis 
    ... stress. Certain medications can also be triggers, including aspirin, opioids, or non-steroidal anti-inflammatory drugs (NSAIDs). ... G, Sperr WR, Wimazal F, Wohrl S, Zahel B, Pehamberger H. Guidelines and diagnostic algorithm for patients ...
    https://medlineplus.gov/genetics/condition/systemic-mastocytosis - Genetics
  9. Very long-chain acyl-CoA dehydrogenase deficiency 
    ... of Reye syndrome occur in children who take aspirin during these viral infections. VLCAD deficiency is estimated ... Apr 2. Citation on PubMed Evans M, Andresen BS, Nation J, Boneh A. VLCAD deficiency: Follow-up ...
    https://medlineplus.gov/...g-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  10. Mitochondrial trifunctional protein deficiency 
    ... Reye syndrome are associated with the use of aspirin during these viral infections. Mitochondrial trifunctional protein deficiency ... de Klerk H, Knerr I, Koch HG, Plecko B, Roschinger W, Schwab KO, Scheible D, Wijburg FA, ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
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