Evaluation of neonatal screening for congenital adrenal hyperplasia

被引:39
作者
Honour, JW
Torresani, T
机构
[1] UCL, Dept Chem Pathol, London W1N 8AA, England
[2] Univ Zurich, Kinderklin, Dept Pediat, CH-8032 Zurich, Switzerland
关键词
congenital adrenal hyperplasia; screening procedures; 21-hydroxylase deficiency;
D O I
10.1159/000049997
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Neonatal screening for congenital hypothyroidism has been effective in early detection and treatment of the condition. The position with respect to neonatal screening for congenital adrenal hyperplasia has been debated for many years. Some countries have performed congenital adrenal hyperplasia screening for many years, others have conducted pilot studies that were then not adopted. This article endeavours to summarize the complex issues behind decisions whether to screen or not and summarizes the findings of neonatal congenital adrenal hyperplasia screening programmes. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:206 / 211
页数:6
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