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6号染色体短臂部分三体性

Partial trisomy 6p.

作者信息

Bernheim A, Berger R, Vaugier G, Thieffry J C, Matet Y

出版信息

Hum Genet. 1979 Apr 17;48(1):13-6. doi: 10.1007/BF00273268.

Abstract

A case of trisomy 6p21 leads to 6pter resulting from a maternal balanced t(2;6)(p25;p21) translocation is reported. The main clinical abnormalities were psychomotor retardation, hypotrophy, blepharophimosis, nystagmus, high nasal bridge, small mouth, sacral dimple, and systolic murmur. Other anomalies might have been due to partial 2p monosomy. Comparison with seven other cases of trisomy 6p allowed the delineation of a clinical entity. Direct proof of the localization of HLA genes was given by the presence of three haplotypes in the index patient.

摘要

报道了一例因母亲平衡易位t(2;6)(p25;p21)导致6p21三体并延伸至6p末端的病例。主要临床异常表现为精神运动发育迟缓、发育不良、睑裂狭小、眼球震颤、鼻梁高、小嘴、骶部酒窝和收缩期杂音。其他异常可能是由于2p部分单体所致。与其他7例6p三体病例的比较,明确了一种临床实体。先证者中存在三种单倍型,直接证明了HLA基因的定位。

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