Inborn errors of metabolism / by Archibald E. Garrod.

  • Archibald Garrod
Date:
1909
Catalogue details

Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: Inborn errors of metabolism / by Archibald E. Garrod. Source: Wellcome Collection.

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    Homogen tisic acid (contin ued),— lead salt of, 49 limited destruction of, in normal organism, 68 parents substances of, 54 in plants, supposed formation of, by action of tyrosin ase, 72 properties of, 50 reaction of, with ferric chloride, 42 synthesis of, 48 Hydroquinone-acetic acid. See Homogentisic Acid Hydro quinone-a-lactic acid, the supposed uroleucic acid, 51 synthesis of, 53 Hydro quinone-pyruvic acid— effect of its administration to an alkaptonuria 78 Inborn errors of metabolism— characters of, 13 congenital occurrence of, 17 conspicuous character of those known, 17 heredity of, 22 persistence of, 17 Indol, origin of from trypto phane, 10 Intermediate products of meta bolism, excretion of, 7, 11 Jewish race— occurrence of pentosuria in, 31, 140, 143 Joints, lesions of, in association with ochronosis and alk aptonuria, 46 Kidneys, diseases of, effect of, upon urinary excretion, 10 selective retention of pro teins by, 3 Kynurenic acid, in urine of dogs, 2 Lactose, effect of administra tion of, to pentosurics, 155 Lsevulose, not dealt with in organism in same way as dextrose, 6 Leucin, as an acetone yielding substance, 61, 81 catabolism of, in alkapton uria, 81 in urine, in acute yellow atrophy of liver, 12 in urine, in cystinuria, 101, 128 Liver, disease of, effect of, on metabolism, 12 formation of acetone in per fused, 61 desamintion in, 134 Lysin, effect of administration of, to a cystinuric, 125 not found in urine in cys tinuria, 127 parent substance of cada- verin, 101, 124 Malformations, structural, com pared to chemical ano malies, 14 structural, classification of, 14 structural, sex incidence of, 20 Melanins— absent in albinism, 35 chemistry of, 35
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