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11号染色体长臂部分缺失[del(11)(q23)]:雅各布森综合征。两例新病例及临床发现回顾。

Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.

作者信息

Schinzel A, Auf der Maur P, Moser H

出版信息

J Med Genet. 1977 Dec;14(6):438-44. doi: 10.1136/jmg.14.6.438.

Abstract

Two cases, a boy and a girl, with the 11q-(Jacobsen) syndrome are reported. Findings common to both and typical for this chromosome aberration include a narrow protruding forehead, hypertelorism, non-horizontal position of the eyes, ptosis, strabismus, broad root, and short upturned tip of thenose, carp mouth, receding chin, misshapen ears, simian creases, and severe mental retardation. In addition, one patient had pyloric stenosis and an inguinal hernia. Growth retardation and microcephaly were not found in either of them. The karyotypes revealed de novo-deletions of the long arm of one chromosome 11,del(11)(q23).

摘要

报道了两例患有11q-(雅各布森)综合征的病例,一男一女。两者共有的、且为此种染色体畸变所特有的表现包括前额狭窄突出、眼距过宽、眼睛非水平位、上睑下垂、斜视、鼻根宽且鼻尖短而上翘、鲤鱼嘴、下巴后缩、耳朵畸形、猿掌纹以及严重智力发育迟缓。此外,一名患者患有幽门狭窄和腹股沟疝。两者均未发现生长发育迟缓及小头畸形。核型分析显示一条11号染色体长臂的新发缺失,即del(11)(q23)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f2d/1013641/15b62c870d1f/jmedgene00307-0051-a.jpg

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