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巨头畸形、眼距过宽、四肢短小、听力丧失和发育迟缓的新综合征。

New syndrome of macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay.

作者信息

Bagatelle R, Cassidy S B

机构信息

Department of Pediatrics, University of Arizona College of Medicine, Tucson, USA.

出版信息

Am J Med Genet. 1995 Jan 30;55(3):367-71. doi: 10.1002/ajmg.1320550324.

Abstract

We describe a boy with an apparently unique constellation of anomalies, including macrocephaly, short stature, relatively short limbs, hearing loss, developmental delay, sparse anterior scalp hair, hypertelorism, downslanting palpebral fissures, and a short nose with a broad, flat nasal bridge and anteverted nares. Chromosomes were normal and radiographs failed to show a bone dysplasia. We conclude that this represents a new syndrome.

摘要

我们描述了一个患有明显独特异常组合的男孩,包括巨头畸形、身材矮小、四肢相对较短、听力丧失、发育迟缓、前头皮毛发稀疏、眼距过宽、睑裂向下倾斜,以及鼻梁宽平且鼻孔前倾的短鼻。染色体正常,X线片未显示骨发育异常。我们得出结论,这代表一种新的综合征。

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