MAPLE SYRUP URINE DISEASE - 4 YEARS EXPERIENCE WITH DIETARY TREATMENT OF A CASE

被引:10
作者
DICKINSON, JP
HOLTON, JB
LEWIS, GM
LITTLEWOOD, JM
STEEL, AE
机构
[1] Departments of Chemical Pathology and of Paediatrics and Child Health, University of Leeds
[2] Department of Pathology, University of Leeds
[3] St. Mary's Hospital, Portsmouth
[4] Department of Pathology, Southmead General Hospital, Bristol
[5] Biochemistry Department, Seacroft
[6] Killingbeck Hospitals, Leeds
来源
ACTA PAEDIATRICA SCANDINAVICA | 1969年 / 58卷 / 04期
关键词
Acidosis; Allo‐isoleucine; Dietary treatment; Errors of metabolism; Maple Syrup Urine Disease;
D O I
10.1111/j.1651-2227.1969.tb04730.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
An infant with Maple Syrup Urine Disease was treated from six weeks of age with a synthetic diet containing carefully restricted quantities of branched chain aminoacids. There was a marked immediate improvement. At twelve weeks, gross vitamin deficiency developed and was corrected. The patient is now more than four‐and‐a‐half years old, and although in reasonable general health is quite severely retarded, both mentally and physically. The problems of diagnosis, the biochemical basis of dietary treatment and the laboratory requirements for control are discussed in relation to the 55 previously published cases. Copyright © 1969, Wiley Blackwell. All rights reserved
引用
收藏
页码:341 / +
页数:1
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