Neonatal screening for congenital hypothyroidism

被引:4
|
作者
Leger, Juliane [1 ]
机构
[1] Univ Paris, HOp Univ Robert Debre, AP HP Nord,Inserm NeuroDiderot,UMR 1141, Serv Endocrinol Diabetol Pediat,Ctr Reference Mal, 48 Blvd Serurier, F-75019 Paris, France
来源
M S-MEDECINE SCIENCES | 2021年 / 37卷 / 05期
关键词
THYROID DYSGENESIS; PREGNANCY; CHILDREN; ASSOCIATION; GUIDELINES; MANAGEMENT; DIAGNOSIS; OUTCOMES; INFANTS; DISEASE;
D O I
10.1051/medsci/2021058
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Congenital hypothyroidism (CH) is the leading cause of preventable mental retardation. It is mainly due to thyroid dysgenesis or dyshormonogenesis with normally located gland, and detected at birth in developed countries by systematic neonatal screening. The early treatment of patients with CH has successfully improved the prognosis and management of this disease. An increase in the incidence of congenital hypothyroidism with a normally located gland has been reported worldwide over the last three decades. The etiology of CH with a normally located gland remains elusive and about half of them demonstrate spontaneous resolution of CH within a few months (transient CH). They highlight the need to reevaluate thyroid function during follow-up.
引用
收藏
页码:474 / 481
页数:8
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