Suppr超能文献

连锁图谱分析和全外显子组测序在一个大型多代家庭中鉴定出CX3CR1基因中的一个共享变异。

Linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in a large multi-generation family.

作者信息

Feldman George J, Parvizi Javad, Sawan Hind, Erickson Jill A, Peters Christopher L

机构信息

Thomas Jefferson University Division of Orthopaedic Research, Philadelphia, PA.

Thomas Jefferson University Division of Orthopaedic Research, Philadelphia, PA; Rothman Institute of Orthopaedics, Philadelphia, PA.

出版信息

J Arthroplasty. 2014 Sep;29(9 Suppl):238-41. doi: 10.1016/j.arth.2014.05.014. Epub 2014 Jun 2.

Abstract

Developmental dysplasia of the hip (DDH) is a crippling condition that affects children and adults, with an average incidence of 1-1.5 cases per 1000 live births. It results in disabling arthritis of the hip in up to 60% patients in the 20-40 year age group. There is no accurate diagnostic test available for newborns. The purpose of our study is to develop a sensitive and specific genetic test for DDH by identifying causative mutations. Linkage analysis and whole exome sequencing of 4 severely affected individuals of a 4 generation 71 member family was performed. The damaging rs3732378 variant in the CX3CR1 chemokine receptor was shared by all affected family members and by 15% of 28 sporadic dysplastics.

摘要

发育性髋关节发育不良(DDH)是一种影响儿童和成人的致残性疾病,平均发病率为每1000例活产中有1 - 1.5例。在20 - 40岁年龄组中,高达60%的患者会因此导致髋关节致残性关节炎。目前尚无针对新生儿的准确诊断测试。我们研究的目的是通过识别致病突变来开发一种针对DDH的敏感且特异的基因检测方法。对一个四代71名成员的家族中的4名严重受影响个体进行了连锁分析和全外显子测序。所有受影响的家庭成员以及28名散发发育不良患者中的15%都存在趋化因子受体CX3CR1中具有损害性的rs3732378变异。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验