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胫骨缺如/发育不全、多指畸形、小脑后蛛网膜囊肿及其他异常:一种常染色体隐性疾病。

Absence/hypoplasia of tibia, polydactyly, retrocerebellar arachnoid cyst, and other anomalies: an autosomal recessive disorder.

作者信息

Holmes L B, Redline R W, Brown D L, Williams A J, Collins T

机构信息

Department of Newborn Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.

出版信息

J Med Genet. 1995 Nov;32(11):896-900. doi: 10.1136/jmg.32.11.896.

Abstract

Absence or hypoplasia of the tibia has been reported to occur as an isolated hereditary malformation as well as a feature of several autosomal recessive and autosomal dominant syndromes. We report three sibs with absence or hypoplasia of the tibia in association with other malformations whose parents are first cousins once removed. These infants appear to have a "new" autosomal recessive syndrome.

摘要

据报道,胫骨缺如或发育不全可作为一种孤立的遗传性畸形出现,也可作为几种常染色体隐性和常染色体显性综合征的特征。我们报告了三例胫骨缺如或发育不全并伴有其他畸形的同胞,其父母是隔了一代的堂(表)亲。这些婴儿似乎患有一种“新的”常染色体隐性综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/397e/1051745/b0c82dfcdeb1/jmedgene00278-0059-a.jpg

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