Suppr超能文献

Coffin-Siris 综合征和 BAF 复合物:63 例患者的基因型-表型研究。

Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients.

机构信息

Center for Human and Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.

出版信息

Hum Mutat. 2013 Nov;34(11):1519-28. doi: 10.1002/humu.22394. Epub 2013 Aug 30.

Abstract

De novo germline variants in several components of the SWI/SNF-like BAF complex can cause Coffin-Siris syndrome (CSS), Nicolaides-Baraitser syndrome (NCBRS), and nonsyndromic intellectual disability. We screened 63 patients with a clinical diagnosis of CSS for these genes (ARID1A, ARID1B, SMARCA2, SMARCA4, SMARCB1, and SMARCE1) and identified pathogenic variants in 45 (71%) patients. We found a high proportion of variants in ARID1B (68%). All four pathogenic variants in ARID1A appeared to be mosaic. By using all variants from the Exome Variant Server as test data, we were able to classify variants in ARID1A, ARID1B, and SMARCB1 reliably as being pathogenic or nonpathogenic. For SMARCA2, SMARCA4, and SMARCE1 several variants in the EVS remained unclassified, underlining the importance of parental testing. We have entered all variant and clinical information in LOVD-powered databases to facilitate further genotype-phenotype correlations, as these will become increasingly important because of the uptake of targeted and untargeted next generation sequencing in diagnostics. The emerging phenotype-genotype correlation is that SMARCB1 patients have the most marked physical phenotype and severe cognitive and growth delay. The variability in phenotype seems most marked in ARID1A and ARID1B patients. Distal limbs anomalies are most marked in ARID1A patients and least in SMARCB1 patients. Numbers are small however, and larger series are needed to confirm this correlation.

摘要

几种 SWI/SNF 样 BAF 复合物成分中的新生种系变异可导致 Coffin-Siris 综合征 (CSS)、Nicolaides-Baraitser 综合征 (NCBRS) 和非综合征性智力障碍。我们对 63 名临床诊断为 CSS 的患者进行了这些基因 (ARID1A、ARID1B、SMARCA2、SMARCA4、SMARCB1 和 SMARCE1) 的筛查,在 45 名 (71%) 患者中发现了致病性变异。我们发现 ARID1B 中的变异比例很高 (68%)。ARID1A 中的所有四个致病性变异似乎都是镶嵌性的。通过使用 Exome Variant Server 中的所有变体作为测试数据,我们能够可靠地将 ARID1A、ARID1B 和 SMARCB1 中的变体分类为致病性或非致病性。对于 SMARCA2、SMARCA4 和 SMARCE1,EVS 中的几个变体仍未分类,这突显了进行父母测试的重要性。我们已经将所有变体和临床信息输入到基于 LOVD 的数据库中,以促进进一步的基因型-表型相关性,因为随着靶向和非靶向下一代测序在诊断中的应用,这些相关性将变得越来越重要。正在出现的表型-基因型相关性是,SMARCB1 患者具有最明显的体格表型和严重的认知和生长延迟。在 ARID1A 和 ARID1B 患者中,表型的可变性似乎最为明显。ARID1A 患者的四肢远端畸形最为明显,而 SMARCB1 患者的四肢远端畸形则最少。然而,数量很少,需要更大的系列来证实这种相关性。

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