3-HYDROXYISOBUTYRIC ACIDURIA - AN INBORN ERROR OF VALINE METABOLISM

被引:27
|
作者
KO, FJ [1 ]
NYHAN, WL [1 ]
WOLFF, J [1 ]
BARSHOP, B [1 ]
SWEETMAN, L [1 ]
机构
[1] UNIV CALIF SAN DIEGO,DEPT PEDIAT,LA JOLLA,CA 92093
关键词
D O I
10.1203/00006450-199110000-00006
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
3-Hydroxyisobutyric aciduria, a disorder of valine metabolism, has been found in a boy in whom the clinical picture was that of a typical organic acidemia with repeated episodes of ketoacidosis requiring admission to hospital and parenteral fluid therapy, along with impressive failure to thrive and chronic lactic acidemia. The excretion of 3-hydroxyisobutyric acid ranged from 170 to 390 mmol/mol of creatinine. The administration of valine increased this to 18 700 mmol/mol of creatinine and reproduced the clinical picture of ketoacidosis. Concentrations of free carnitine were low, and esterified carnitine was elevated. Treatment with carnitine and a diet restricted in protein appeared to be beneficial.
引用
收藏
页码:322 / 326
页数:5
相关论文
共 50 条
  • [31] Evidence that 3-hydroxyisobutyric acid inhibits key enzymes of energy metabolism in cerebral cortex of young rats
    Viegas, Carolina Maso
    Ferreira, Gustavo da Costa
    Schuck, Patricia Fernanda
    Tonin, Anelise Miotti
    Zanatta, Angela
    Wyse, Angela Terezinha de Souza
    Dutra-Filho, Carlos Severo
    Duval Wannmacher, Clovis Milton
    Wajner, Moacir
    INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2008, 26 (3-4) : 293 - 299
  • [32] METHYLMALONIC ACIDURIA - A NEWLY DISCOVERED INBORN ERROR
    BARNESS, LA
    MORROW, G
    ANNALS OF INTERNAL MEDICINE, 1968, 69 (03) : 633 - +
  • [33] ALPHA-KETOADIPIC ACIDURIA, A NEW INBORN ERROR OF LYSINE METABOLISM - BIOCHEMICAL STUDIES
    PRZYREMBEL, H
    BACHMANN, D
    LOMBECK, I
    BECKER, K
    WENDEL, U
    WADMAN, SK
    BREMER, HJ
    CLINICA CHIMICA ACTA, 1975, 58 (03) : 257 - 269
  • [34] BETA-HYDROXYISOVALERIC ACIDURIA AND BETA-METHYLCROTONYLGLYCINURIA - A NEW INBORN ERROR OF METABOLISM
    ELDJARN, L
    JELLUM, E
    STOKKE, O
    PANDE, H
    WAALER, PE
    LANCET, 1970, 2 (7671): : 521 - &
  • [35] ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolism
    Peters, Heidi
    Buck, Nicole
    Wanders, Ronald
    Ruiter, Jos
    Waterham, Hans
    Koster, Janet
    Yaplito-Lee, Joy
    Ferdinandusse, Sacha
    Pitt, James
    BRAIN, 2014, 137 : 2903 - 2908
  • [36] Inborn error of metabolism
    Boyana Konforti
    Nature Structural Biology, 2000, 7 (7) : 535 - 536
  • [37] Inborn error of metabolism
    Konforti, B
    NATURE STRUCTURAL BIOLOGY, 2000, 7 (07): : 535 - 536
  • [38] Structure, interactions and action of Mycobacterium tuberculosis 3-hydroxyisobutyric acid dehydrogenase
    Srikalaivani, Rajapiramuthu
    Singh, Amrita
    Vijayan, Mamannamana
    Surolia, Avadhesha
    BIOCHEMICAL JOURNAL, 2018, 475 : 2457 - 2471
  • [39] MEVALONIC ACIDURIA - AN INBORN ERROR OF CHOLESTEROL-BIOSYNTHESIS
    BERGER, R
    SMIT, GPA
    SCHIERBEEK, H
    BIJSTERVELD, K
    LECOULTRE, R
    CLINICA CHIMICA ACTA, 1985, 152 (1-2) : 219 - 222
  • [40] 4-HYDROXYBUTYRIC ACIDURIA - A NEW INBORN ERROR OF METABOLISM .2. BIOCHEMICAL FINDINGS
    JAKOBS, C
    KNEER, J
    RATING, D
    HANEFELD, F
    DIVRY, P
    HERMIER, M
    JOURNAL OF INHERITED METABOLIC DISEASE, 1984, 7 : 92 - 94