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布腊克曼-德朗热综合征。临床表型的描述。

Brachmann-de Lange syndrome. Delineation of the clinical phenotype.

作者信息

Ireland M, Donnai D, Burn J

机构信息

Department of Human Genetics, University of Newcastle Upon Tyne, United Kingdom.

出版信息

Am J Med Genet. 1993 Nov 15;47(7):959-64. doi: 10.1002/ajmg.1320470705.

Abstract

A total of 31 cases previously diagnosed as having Brachmann-de Lange syndrome were ascertained and examined, of which 11 were thought to have been misdiagnosed. Of those correctly diagnosed, there appeared to be a phenotypic dichotomy with classical and mild cases. Those facial findings of greatest diagnostic value were the combination of the characteristic eyebrows, long philtrum, thin lips and crescent-shaped mouth. The characteristic eyebrows were neat, well defined and arched as though they had been pencilled. This combination of anomalies was absent in postpubertal males but not in postpubertal females. Facial abnormalities most likely to lead to incorrect use of the eponym were hypertrichosis, synophrys, and bushy eyebrows.

摘要

共确定并检查了31例先前被诊断为患有布-德综合征的病例,其中11例被认为是误诊。在那些被正确诊断的病例中,似乎存在经典型和轻型病例的表型二分法。最具诊断价值的面部表现是特征性眉毛、长人中、薄唇和新月形嘴的组合。特征性眉毛整齐、轮廓清晰且呈拱形,仿佛是用眉笔画出来的。这种异常组合在青春期后男性中不存在,但在青春期后女性中存在。最有可能导致错误使用该名称的面部异常是多毛症、连眉和浓密眉毛。

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