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A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report

机译:患有癫痫,ID和自闭症谱系障碍的女性患者的15q染色体微缺失:一例报告

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Key Clinical Message 15q deletions have been described in association with intellectual disability and autism spectrum disorder (ASD). Previous reports have supported the role of 15q24 low copy repeats (LCRs) in mediating alternatively sized genomic rearrangements. Based on our reported finding of a 15q24 deletion coinciding with two LCR regions in a patient with epilepsy and ASD, we recommend that patients with 15q24 deletions be evaluated for ASD for early institution of therapy.
机译:已将关键临床消息15q缺失与智力障碍和自闭症谱系障碍(ASD)相关联进行了描述。以前的报道支持15q24低拷贝重复序列(LCR)在介导大小可变的基因组重排中的作用。基于我们报告的发现癫痫和ASD患者的15q24缺失与两个LCR区域重合的发现,我们建议对15q24缺失的患者进行ASD评估,以及早治疗。

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