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由于1q间质缺失导致的多发性先天性异常/智力障碍(MCA/MR)综合征

Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.

作者信息

Steinbach P, Wolf M, Schmidt H

出版信息

Am J Med Genet. 1984 Sep;19(1):131-6. doi: 10.1002/ajmg.1320190114.

Abstract

A severely retarded male infant was found to have a previously undescribed multiple congenital anomalies/mental retardation (MCA/MR) syndrome including microdolichocephaly, prominence of metopic suture, coarse scalp hair, epicanthus, anteverted nostrils, micrognathia, posteriorly angulated malformed auricles, preaxial hexadactyly, clinodactyly, camptodactyly, hypospadias, cryptorchidism, inguinal hernias, agenesis of left kidney, and pyloric stenosis. This syndrome was due to an interstitial del(1)(q25.2q31.2) associated with a paracentric inv(1)(q31.2q44).

摘要

一名重度智力发育迟缓的男婴被发现患有此前未描述过的多种先天性异常/智力发育迟缓(MCA/MR)综合征,包括小头长头畸形、额缝突出、头皮毛发粗糙、内眦赘皮、鼻孔前倾、小颌畸形、耳廓向后成角畸形、轴前多指畸形、小指内弯、屈曲指、尿道下裂、隐睾、腹股沟疝、左肾缺如和幽门狭窄。该综合征是由一个与臂间倒位inv(1)(q31.2q44)相关的间质性缺失del(1)(q25.2q31.2)所致。

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