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Analysis of chromosomal abnormalities by CGH-array in patients with dysmorphic and intellectual disability with normal karyotype

机译:核心型瘤症患者患者CGH系列染色体异常分析

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摘要

ABSTRACT Objective To investigate chromosomal abnormalities by CGH-array in patients with dysmorphic features and intellectual disability with normal conventional karyotype. Methods Retrospective study, carried out from January 2012 to February 2014, analyzing the CGH-array results of 39 patients. Results Twenty-six (66.7%) patients had normal results and 13 (33.3%) showed abnormal results - in that, 6 (15.4%) had pathogenic variants, 6 (15.4%) variants designated as uncertain and 1 (2.5%) non-pathogenic variants. Conclusion The characterization of the genetic profile by CGH-array in patients with intellectual disability and dysmorphic features enabled making etiologic diagnosis, followed by genetic counseling for families and specific treatment.
机译:摘要目的探讨CGH阵列患者疑难生特征和智障型核心型核心型核心异常的染色体异常。方法回顾性研究,从2012年1月到2014年2月进行,分析了39名患者的CGH阵列结果。结果26例(66.7%)的患者具有正常的结果,13例(33.3%)显示出异常结果 - 其中,6(15.4%)具有致病变体,6(15.4%)变体指定为不确定,1(2.5%)非 - 植物变异。结论智力残疾患者CGH系列遗传谱的表征能够使病因诊断,其次是家庭和特定治疗的遗传咨询。

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