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[一名7岁中度智力发育迟缓女孩的近端4p综合征]

[Proximal 4p syndrome in a 7-year-old moderately retarded girl].

作者信息

Volleth M, Erhardt J, Schmitzer E, Pfeiffer R A

机构信息

Institut für Humangenetik, Friedrich-Alexander-Universität Erlangen-Nürnberg.

出版信息

Monatsschr Kinderheilkd. 1993 Aug;141(8):655-8.

PMID:8377770
Abstract

A 7 year old girl in whom an interstitial deletion of the short arm of a chromosome no. 4 had been discovered [46, XX, del(4)(p15.2p16)] is moderately retarded and exhibits some mild craniofacial dysmorphies. Cardiological examination revealed a PDA and an ASD. From seven similar cases published up to now a typical phenotype cannot be concluded. Dermatoglyphics show a remarkable frequency of digital arches but the diagnostic significance is questioned by this observation.

摘要

一名7岁女孩被发现存在4号染色体短臂的间质缺失[46, XX, del(4)(p15.2p16)],她中度智力发育迟缓,并有一些轻度的颅面畸形。心脏检查发现有动脉导管未闭和房间隔缺损。从目前已发表的7个类似病例中,无法得出典型的表型。皮纹学显示指纹弓出现频率显著,但这一观察结果对其诊断意义提出了质疑。

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