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[先天性甲状腺功能减退症筛查异常新生儿及儿童先天性甲状腺功能减退症临床诊疗模型]

[A model for clinical diagnosis-treatment of the newborn with an abnormal screening test for hypothyroidism and in children with congenital hypothyroidism].

作者信息

Szymborska M

机构信息

Zaklad Endokrynologii, Instytut Matki i Dziecka, Kasprzaka 17a, 01-211, Warszawa, Poland.

出版信息

Med Wieku Rozwoj. 2000 Oct-Dec;4(4):467-74.

Abstract

Congenital hypothyroidism occurs in 1:4000 newborns. Mass screening for congenital hypothyroidism constitutes a major progress in the prevention of mental retardation. The neonatal screening programme in Poland was established and implemented by the National Research Institute of Mother and Child from the middle of the 70. and reorganised in 1997. Recall examinations in the infants, substitute therapy with l-thyroxine and the follow-up of hypothyroid infants and children are presented.

摘要

先天性甲状腺功能减退症在每4000名新生儿中出现1例。先天性甲状腺功能减退症的大规模筛查是预防智力迟钝方面的一项重大进展。波兰的新生儿筛查计划由国家母婴研究所于70年代中期制定并实施,并于1997年进行了重组。本文介绍了对婴儿的召回检查、左甲状腺素替代治疗以及甲状腺功能减退症婴幼儿的随访情况。

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