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外耳道闭锁、肩胛肱骨骨性连接及其他骨骼异常:常染色体隐性“萨姆斯”综合征的确诊

Auditory canal atresia, humeroscapular synostosis, and other skeletal abnormalities: confirmation of the autosomal recessive "SAMS" syndrome.

作者信息

ter Heide Henriette, Bulstra Sjoerd K, Reekers Ad, Schrander Jaap J P, Schrander-Stumpel Constance T R M

机构信息

Department of Pediatrics, Academic Hospital Maastricht, Maastricht, The Netherlands.

出版信息

Am J Med Genet. 2002 Jul 15;110(4):359-64. doi: 10.1002/ajmg.10441.

Abstract

A second girl with the unique combination of auditory canal atresia and scapulohumeral synostosis is reported. This patient also had bilateral clubfeet and genital abnormalities. The other patient reported with this syndrome and the presently reported child both had consanguineous parents. Mental development was normal in both children. The acronym SAMS (Short stature, Auditory canal atresia, Mandibular hypoplasia, and Skeletal abnormalities) was suggested to describe the main manifestations in this syndrome.

摘要

报道了第二例患有外耳道闭锁和肩胛肱骨骨性连接这一独特组合病症的女孩。该患者还患有双侧畸形足和生殖器异常。此前报道的患有此综合征的另一名患者以及目前报道的这名儿童的父母均为近亲。两名儿童的智力发育均正常。有人建议用首字母缩略词SAMS(身材矮小、外耳道闭锁、下颌发育不全和骨骼异常)来描述该综合征的主要表现。

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