Suppr超能文献

一名患有inv dup del(9p)和22q11.2微重复的儿童的多小脑回畸形。

Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplication.

作者信息

Mosca A L, Callier P, Faivre L, Marle N, Mejean N, Thauvin-Robinet C, Masurel-Paulet A, Madinier N, Durand C, Couillaud G, Ragot S, Huet F, Teyssier J R, Mugneret F

机构信息

Département de Génétique, CHU le Bocage, Dijon, France.

出版信息

Am J Med Genet A. 2009 Mar;149A(3):475-81. doi: 10.1002/ajmg.a.32665.

Abstract

Polymicrogyria (PMG) is a relatively common malformation of the cortex for which the pathogenesis remains poorly understood. Both acquired and genetic causes are known, and to date more than 70 cases of PMG have been associated with chromosomal abnormalities. Here we report on a 12-year-old girl presenting with asymmetrical PMG predominantly affecting the right occipital lobe. She was the only child of consanguineous parents. At 7 years of age she was referred for mental retardation with speech delay and seizures. Cytogenetic studies of the patient revealed an inverted 9p duplication/deletion and bacterial artificial chromosomes (BACs)-array also showed a 22q11.2 microduplication confirmed by quantitative PCR. This case is of interest in the search for candidate genes and emphasizes the importance of the 22q11 region in PMG. It also highlights the efficiency of BACs-array in detecting complex rearrangements.

摘要

多小脑回畸形(PMG)是一种相对常见的皮质发育畸形,其发病机制仍知之甚少。已知有后天性和遗传性病因,迄今为止,已有70多例PMG与染色体异常有关。在此,我们报告一名12岁女孩,表现为不对称性PMG,主要累及右侧枕叶。她是近亲结婚父母的独生女。7岁时,她因智力发育迟缓、语言发育延迟和癫痫发作而就诊。对该患者的细胞遗传学研究显示9号染色体短臂倒置重复/缺失,细菌人工染色体(BAC)阵列也显示22q11.2微重复,经定量PCR证实。该病例对于寻找候选基因具有重要意义,并强调了22q11区域在PMG中的重要性。它还突出了BAC阵列在检测复杂重排方面的效率。

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