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塞克尔综合征:一种被过度诊断的综合征。

Seckel syndrome: an overdiagnosed syndrome.

作者信息

Thompson E, Pembrey M

出版信息

J Med Genet. 1985 Jun;22(3):192-201. doi: 10.1136/jmg.22.3.192.

Abstract

Five children in whom a diagnosis of Seckel syndrome had previously been made were re-examined in the genetic unit. One child had classical Seckel syndrome, a sib pair had the features of the syndrome with less severe short stature, and in two children the diagnosis was not confirmed. Seckel syndrome is only one of a group of low birth weight microcephalic dwarfism and careful attention should be paid to fulfillment of the major criteria defined by Seckel before the diagnosis is made. There remains a heterogeneous group of low birth weight microcephalic dwarfism yet to be defined.

摘要

曾被诊断为塞克尔综合征的5名儿童在遗传科接受了重新检查。1名儿童患有典型的塞克尔综合征,1对同胞具有该综合征特征但身材矮小程度较轻,另有2名儿童的诊断未得到证实。塞克尔综合征只是低出生体重小头侏儒症群体中的一种,在做出诊断前应仔细关注塞克尔所定义的主要标准是否满足。仍有一组异质性的低出生体重小头侏儒症有待明确。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc34/1049424/9032470feef2/jmedgene00095-0033-a.jpg

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