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Chiari畸形的家族聚集性:病例报告、家系分析及文献综述

Familial Aggregation of Chiari Malformation: Presentation, Pedigree, and Review of the Literature.

作者信息

Nagy Laszlo, Mobley James, Ray Coby

机构信息

Texas Tech University, Health Sciences Center, Texas, USA.

出版信息

Turk Neurosurg. 2016;26(2):315-20. doi: 10.5137/1019-5149.JTN.10471-14.1.

Abstract

This article reports the largest familial aggregation of Chiari malformation in a single family to date as reported in the literature. This study is a retrospective case series of a family of whom five individuals have a confirmed case of Chiari malformation and three additional individuals have Chiari signs and symptoms. This contribution further supports the implication of genetics in the transmission of Chiari malformation. The family reported in this study also has a significant incidence of Ehlers-Danlos. Three sisters, including a set of twins, presented with confirmed cases of Chiari malformation and four of the five children of the twin sisters presented with confirmed or suspected Chiari malformation. Of note, the non-twin sister has three children who are unaffected. This report provides further evidence for a shared loci between the Chiari malformation and Ehlers-Danlos.

摘要

本文报道了文献中迄今单个家族中最大的小脑扁桃体下疝畸形家族聚集病例。本研究是一个回顾性病例系列,该家族中有5人确诊为小脑扁桃体下疝畸形,另有3人有小脑扁桃体下疝畸形的体征和症状。这一发现进一步支持了遗传学在小脑扁桃体下疝畸形传播中的作用。本研究报道的这个家族中埃勒斯-当洛综合征的发病率也很高。三姐妹,包括一对双胞胎,被确诊为小脑扁桃体下疝畸形,双胞胎姐妹的5个孩子中有4个被确诊或疑似患有小脑扁桃体下疝畸形。值得注意的是,非双胞胎姐妹有3个未受影响的孩子。本报告为小脑扁桃体下疝畸形和埃勒斯-当洛综合征之间存在共同基因座提供了进一步证据。

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