Suppr超能文献

患有广泛多样临床表现的腭心面综合征患者的22号染色体q11.2微缺失

Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.

作者信息

Ravnan J B, Chen E, Golabi M, Lebo R V

机构信息

Department of Pediatrics, University of California, San Francisco, USA.

出版信息

Am J Med Genet. 1996 Dec 18;66(3):250-6. doi: 10.1002/(SICI)1096-8628(19961218)66:3<250::AID-AJMG2>3.0.CO;2-T.

Abstract

Velocardiofacial syndrome (VCFS) and the DiGeorge sequence (DGS) are caused by 22q11.2 deletions. Fluorescence in situ hybridization (FISH) using the DiGeorge chromosome region (DGCR) probe (Oncor) was used to detect 31 deletions in 100 patients with possible VCFS. Retrospective FISH analysis of archived slides from 14 patients originally studied only by high-resolution G banding detected 6 patients with a DGCR deletion, and only 2 of these 6 had a microscopically visible chromosome deletion. The 4 familial deletions found exhibited a wide range of clinical presentations within each family. Comparison of clinical characteristics of patients with and without the DGCR deletion determined findings predictive of the deletion: abundant or unruly scalp hair; narrow palpebral fissures; a laterally "built-up" nose; velopharyngeal inadequacy; thymic hypoplasia; and congenital heart defects, specifically tetralogy of Fallot, ventriculoseptal defect, and interrupted aortic arch.

摘要

腭心面综合征(VCFS)和迪乔治序列征(DGS)由22q11.2缺失引起。使用迪乔治染色体区域(DGCR)探针(Oncor)进行荧光原位杂交(FISH),以检测100例可能患有VCFS的患者中的31例缺失。对最初仅通过高分辨率G显带研究的14例患者的存档玻片进行回顾性FISH分析,发现6例患者存在DGCR缺失,其中这6例中只有2例在显微镜下可见染色体缺失。发现的4例家族性缺失在每个家族中表现出广泛的临床表现。对有和没有DGCR缺失的患者的临床特征进行比较,确定了预测缺失的发现:头皮毛发浓密或杂乱;睑裂狭窄;鼻子呈侧向“堆积”状;腭咽功能不全;胸腺发育不全;以及先天性心脏缺陷,特别是法洛四联症、室间隔缺损和主动脉弓中断。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验