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Results 1 - 10 of 11 for ARGININE OR GLYCERIN OR HYALURONIC ACID OR RETINOL
  1. Caffey disease 
    ... Caffey disease replaces the protein building block (amino acid) arginine with the amino acid cysteine at protein position 836 (written as Arg836Cys ...
    https://medlineplus.gov/genetics/condition/caffey-disease - Genetics
  2. Arginine:glycine amidinotransferase deficiency 
    ... and hydrogen atoms called a guanidino group from arginine to glycine. Guanidinoacetic acid is converted to creatine in the second step of the process. Creatine is needed for the body to store and use energy properly.GATM ... amidinotransferase enzyme to participate in creatine synthesis, ...
    https://medlineplus.gov/...nineglycine-amidinotransferase-deficiency - Genetics
  3. Glutaric acidemia type I 
    ... Burgard P. Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I - A decade ... efficacy and physiological actions of a lysine-free, arginine-rich formula to ... focus on cerebral amino acid influx. Mol Genet Metab. 2011 Sep-Oct;104( ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics
  4. Argininosuccinic aciduria 
    ... to start the reaction in which the amino acid arginine, a building block of proteins, is produced from ...
    https://medlineplus.gov/genetics/condition/argininosuccinic-aciduria - Genetics
  5. Arginase deficiency 
    ... is an inherited disorder that causes the amino acid arginine (a building block of proteins) and ammonia to ...
    https://medlineplus.gov/genetics/condition/arginase-deficiency - Genetics
  6. Lysinuric protein intolerance 
    ... digest and use certain protein building blocks (amino acids), namely lysine, arginine, and ornithine. Because the body cannot absorb these ... LAT-1 protein disrupt the transportation of lysine, arginine, and ornithine. As a result, these amino acids are not absorbed by cells in the small ...
    https://medlineplus.gov/.../condition/lysinuric-protein-intolerance - Genetics
  7. Spondyloepiphyseal dysplasia with metatarsal shortening 
    ... metatarsal shortening replaces one protein building block (amino acid) known as arginine in the COL2A1 protein with another amino acid known as cysteine. This COL2A1 gene variant interferes ...
    https://medlineplus.gov/...seal-dysplasia-with-metatarsal-shortening - Genetics
  8. Guanidinoacetate methyltransferase deficiency 
    ... compound creatine from the protein building blocks (amino acids) glycine, arginine, and methionine. Specifically, guanidinoacetate methyltransferase controls the second ...
    https://medlineplus.gov/...idinoacetate-methyltransferase-deficiency - Genetics
  9. Miller syndrome 
    ... Citation on PubMed Brosnan ME, Brosnan JT. Orotic acid excretion and arginine metabolism. J Nutr. 2007 Jun;137(6 Suppl ...
    https://medlineplus.gov/genetics/condition/miller-syndrome - Genetics
  10. Hyperlysinemia 
    ... D. Biomarkers identified in inborn errors for lysine, arginine, and ornithine. J Nutr. 2007 Jun;137(6 Suppl 2):1669S-1672S. doi: 10.1093/jn/137.6.1669S. Citation on PubMed
    https://medlineplus.gov/genetics/condition/hyperlysinemia - Genetics
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