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新发7号染色体长臂缺失的致死性表现。

A lethal presentation of de novo deletion 7q.

作者信息

McMorrow L E, Toth I R, Gluckson M M, Leff A, Wolman S R

机构信息

Department of Pathology, New York University Medical Center, NY 10016.

出版信息

J Med Genet. 1987 Oct;24(10):629-31. doi: 10.1136/jmg.24.10.629.

Abstract

Deletion of 7q32----qter is a well defined syndrome which usually arises de novo. The proband we report was the result of an uncomplicated 36 week first pregnancy of non-consanguineous Oriental parents. The male infant died shortly after birth. Chromosome studies of peripheral blood and umbilical cord revealed 46,XY,del(7), apparently (q32----qter). The parents' karyotypes were normal. The observed facial structural abnormalities and hydrocephalus rather than microcephaly are in sharp contrast to the clinically described syndrome. The lethal components, absence of suprarenal glands and hydranencephaly, suggest either an unknown confounding factor or a more proximal deletion with an alternative interpretation of 7q--(q23.1----q36.1) rather than the apparent breakpoint at 7q32.

摘要

7q32----qter缺失是一种明确的综合征,通常为新发。我们报告的先证者是一对非近亲的东方父母首次怀孕36周的正常产儿。男婴出生后不久死亡。外周血和脐带的染色体研究显示为46,XY,del(7),明显为(q32----qter)。父母的核型正常。观察到的面部结构异常和脑积水而非小头畸形与临床描述的综合征形成鲜明对比。致命的表现,即肾上腺缺如和积水性无脑畸形,提示存在未知的混杂因素,或7q--(q23.1----q36.1)更靠近近端的缺失,而非7q32处明显的断点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3268/1050293/9642e1195049/jmedgene00084-0054-a.jpg

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