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Results 1 - 10 of 10 for AMMONIA 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. Beta-ureidopropionase deficiency 
    ... down N-carbamyl-beta-alanine to beta-alanine, ammonia, and carbon dioxide. Both beta-aminoisobutyric acid and ... J, Krumpel M, Selim LA, Rashed MS, Assmann B, Meinsma R, Lohkamp B, Ito T, Abeling NG, ...
    https://medlineplus.gov/.../beta-ureidopropionase-deficiency - Genetics
  9. Carnitine-acylcarnitine translocase deficiency 
    ... People with CACT deficiency also usually have excess ammonia in the blood (hyperammonemia), an enlarged liver (hepatomegaly), ... F, Baratta S, Pons R, Chung W, Garavaglia B, Dionisi-Vici C, Ribes A, Parini R, Huertas ...
    https://medlineplus.gov/...tine-acylcarnitine-translocase-deficiency - Genetics
  10. Asparagine synthetase deficiency 
    ... of proteins, asparagine helps to break down toxic ammonia within cells, is important for protein modification, and ... PubMed Ruzzo EK, Capo-Chichi JM, Ben-Zeev B, Chitayat D, Mao H, Pappas AL, Hitomi Y, ...
    https://medlineplus.gov/.../asparagine-synthetase-deficiency - Genetics