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来自高度近亲婚配人群的自闭症谱系障碍患者队列中染色体微阵列分析的诊断率

Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population.

作者信息

Al-Mamari Watfa, Al-Saegh Abeer, Al-Kindy Adila, Bruwer Zandre, Al-Murshedi Fathiya, Al-Thihli Khalid

机构信息

Genetics Department, College of Medicine, Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, PO Box 35, 123, Muscat, Sultanate of Oman.

出版信息

J Autism Dev Disord. 2015 Aug;45(8):2323-8. doi: 10.1007/s10803-015-2394-9.

Abstract

Autism Spectrum Disorders are a complicated group of disorders characterized with heterogeneous genetic etiologies. The genetic investigations for this group of disorders have expanded considerably over the past decade. In our study we designed a tired approach and studied the diagnostic yield of chromosomal microarray analysis on patients referred to the Genetic and Developmental Medicine clinic in Sultan Qaboos University in Oman for autism spectrum disorders in a highly consanguineous population. Copy number variants were seen in 27% of our studied cohort of patients and it was strongly associated with dysmorphic features and congenital anomalies.

摘要

自闭症谱系障碍是一组复杂的疾病,具有异质性的遗传病因。在过去十年中,针对这组疾病的基因研究有了相当大的扩展。在我们的研究中,我们设计了一种分层方法,研究了在阿曼苏丹卡布斯大学遗传与发育医学诊所就诊的、来自高度近亲通婚人群的自闭症谱系障碍患者的染色体微阵列分析的诊断率。在我们研究的患者队列中,27%发现了拷贝数变异,并且它与畸形特征和先天性异常密切相关。

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