Outcome of tyrosinaemia type III

被引:43
作者
Ellaway, CJ
Holme, E
Standing, S
Preece, MA
Green, A
Ploechl, E
Ugarte, M
Trefz, FK
Leonard, JV
机构
[1] Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1N 1EH, England
[2] Sahlgrenska Univ Hosp, Dept Clin Chem & Transfus Med, Gothenburg, Sweden
[3] John Radcliffe Hosp, Dept Clin Biochem, Oxford OX3 9DU, England
[4] Birmingham Childrens Hosp, Dept Clin Chem, Birmingham, W Midlands, England
[5] St Johanns Hosp, Dept Clin Genet, Salzburg, Austria
[6] Univ Autonoma Madrid, Dept Biol Mol, E-28049 Madrid, Spain
[7] Univ Tubingen, Childrens Hosp, Reutlingen Sch Med, D-72074 Tubingen, Germany
关键词
D O I
10.1023/A:1013936107064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tyrosinaemia type III is a rare disorder caused by a deficiency of 4-hydroxyphenylpyruvate dioxygenase, the second enzyme in the catabolic pathway of tyrosine. The majority of the nine previously reported patients have presented with neurological symptoms after the neonatal period, while others detected by neonatal screening have been asymptomatic. All have had normal liver and renal function and none has skin or eye abnormalities. A further four patients with tyrosinaemia type III are described. It is not clear whether a strict low tyrosine diet alters the natural history of tyrosinaemia type III, although there remains a suspicion that treatment may be important, at least in infancy.
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页码:824 / 832
页数:9
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