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科芬-洛里综合征的早期临床体征。

Early clinical signs in Coffin-Lowry syndrome.

作者信息

Vles J S, Haspeslagh M, Raes M M, Fryns J P, Casaer P, Eggermont E

出版信息

Clin Genet. 1984 Nov;26(5):448-52. doi: 10.1111/j.1399-0004.1984.tb01087.x.

Abstract

Two unrelated patients with Coffin-Lowry syndrome are described. The main characteristics of a typical face, thick hands with tapering fingers and a transverse hypothenar crease, general hypotonia with extensible joints made diagnosis possible before the age of 6 months. A persistent large anterior fontanel beyond the age of two years may be another associated finding. Retarded bone age, coarsity of the face and skeletal malformations considered characteristic in adult patients were not present. Early recognition of Coffin-Lowry syndrome is important for genetic counseling and prevention of severe skeletal malformations.

摘要

本文描述了两名患有科芬-洛里综合征的非亲缘关系患者。典型面容、手指呈锥形的厚实双手以及横贯小鱼际的横纹、关节可伸展的全身肌张力减退等主要特征,使得在6个月龄前即可做出诊断。两岁后前囟持续增大可能是另一个相关表现。成人患者典型的骨龄延迟、面容粗糙和骨骼畸形并不存在。早期识别科芬-洛里综合征对于遗传咨询和预防严重骨骼畸形很重要。

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