Suppr超能文献

14q22.3-q23.2 片段缺失:基因型-表型相关性。

Interstitial deletion 14q22.3-q23.2: genotype-phenotype correlation.

机构信息

Departamento de Farmacología, Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain; Spanish Collaborative Study of Congenital Malformations (ECEMC), CIAC (Research Center on Congenital Anomalies), Instituto de Salud Carlos III, Madrid, Spain; CIBER de Enfermedades Raras (CIBERER) (U724), Instituto de Salud Carlos III, Ministerio de Economía y Competitividad, Madrid, Spain.

出版信息

Am J Med Genet A. 2014 Mar;164A(3):639-47. doi: 10.1002/ajmg.a.36330. Epub 2013 Dec 19.

Abstract

The increasing use of molecular tools in genetic diagnosis has produced a surge in the detection of genomic imbalances. Among the growing number of newly discovered chromosome alterations are the interstitial deletions 14q21-q23. In previous reports of this deletion, the patients appear to share ocular defects, pituitary alterations and hand/foot anomalies. Here, we present a 12-year-old girl with dysmorphic face, choanal atresia, gastroesophageal reflux, and moderate developmental delay, in whom an interstitial deletion 14q22.3-q23.2 was detected using a 180k array comparative genome hybridization. The 6.5 Mb deletion contains 27 genes, including three genes of the SIX family: SIX1, SIX4, and SIX6. In mammals, Six1 has been shown to be involved in ocular differentiation, whereas Six4 and Six6 are primarily expressed in the hypothalamus, pituitary gland, and facial bones. We used data on mouse embryos to evaluate the expression of the SIX genes, as well as other representative genes lost in the current patient and a previously published case with a similar phenotype, in order to correlate their pattern of expression with the functional anomalies that constitute the patient's phenotype. We also explored the possibility of other genetic influences, such as the existence of an imprinted region in chromosome 14q, which may provide a better understanding of the observed clinical variability.

摘要

分子工具在遗传诊断中的应用日益广泛,导致基因组不平衡的检测数量激增。在越来越多新发现的染色体改变中,包括 14q21-q23 染色体的中间缺失。在以前关于这种缺失的报道中,患者似乎都有眼部缺陷、垂体改变和手/足畸形。在这里,我们介绍了一位 12 岁的女孩,她有畸形的脸、后鼻孔闭锁、胃食管反流和中度发育迟缓,使用 180k 阵列比较基因组杂交技术检测到 14q22.3-q23.2 染色体的中间缺失。6.5Mb 的缺失包含 27 个基因,包括 SIX 家族的三个基因:SIX1、SIX4 和 SIX6。在哺乳动物中,已经表明 Six1 参与了眼部分化,而 Six4 和 Six6 主要在下丘脑、垂体和面部骨骼中表达。我们使用了关于小鼠胚胎的数据来评估 SIX 基因以及当前患者和以前发表的具有相似表型的患者中丢失的其他代表性基因的表达情况,以便将它们的表达模式与构成患者表型的功能异常相关联。我们还探讨了其他遗传影响的可能性,例如 14q 染色体上印迹区域的存在,这可能有助于更好地理解观察到的临床变异性。

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