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Excretion of galactitol in the urine of heterozygotes of both forms of galactosemia.

作者信息

Sitzmann F C, Schmid R D, Kaloud H

出版信息

Clin Chim Acta. 1977 Mar 1;75(2):313-9. doi: 10.1016/0009-8981(77)90202-9.

DOI:10.1016/0009-8981(77)90202-9
PMID:191219
Abstract

In 36 heterozygotes with Gal-1-PUT deficiency and 3 heterozygotes with galactokinase deficiency galactitol (and galactose) was determined in the urine 2 and 4 h after an intravenous injection of 350 mg galactose/kg body weight (maximum dosis in adults 16 g). For the sake of comparison 10 healthy children and 5 adults, also 4 homozygotes with Gal-1-PUT deficiency and one sick child with galactokinase deficiency were included in this study. The heterozygotes with Gal-1-PUT deficiency demonstrated the same galactitol excretion as the healthy probands, while heterozygotes with galactokinase deficiency excreted a four-fold higher quantity of galactitol than the healthy and heterozygous probands of Gal-1-PUT deficiency. The child with the galactokinase deficiency excreted galactitol for a period of more than 24 h. These results are discussed.

摘要

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引用本文的文献

1
Renal excretion of galactose and galactitol in patients with classical galactosaemia, obligate heterozygous parents and healthy subjects.经典型半乳糖血症患者、 obligate 杂合子父母及健康受试者中半乳糖和半乳糖醇的肾脏排泄情况
J Inherit Metab Dis. 2003;26(5):459-79. doi: 10.1023/a:1025173311030.
2
Clinical features of galactokinase deficiency: a review of the literature.半乳糖激酶缺乏症的临床特征:文献综述
J Inherit Metab Dis. 2002 Dec;25(8):629-34. doi: 10.1023/a:1022875629436.
3
Galactose intolerance and the risk of cataract.半乳糖不耐受与患白内障的风险。
Br J Ophthalmol. 1982 Jul;66(7):438-41. doi: 10.1136/bjo.66.7.438.
4
Inexplicable infantile cataracts and partial maternal galactose disorder.不明原因的婴儿白内障和部分母体半乳糖代谢紊乱。
Arch Dis Child. 1986 May;61(5):445-8. doi: 10.1136/adc.61.5.445.