智力残疾患者的POLR3A罕见变体,心动步态和皮质形:一个病例报告

Caterina Angela Florio1, Federica Mirabella2, Adriana Prato1

  • 1Child and Adolescent Neurology and Psychiatric Section, Azienda Ospedaliera Universitaria Policlinico 'G. Rodolico-San Marco', Department of Clinical and Experimental Medicine, University of Catania, Catania, 95124, Italy.

PubMed
概括

这项研究呈现了一例异常表现的儿童中与POLR3A相关的疾病病例,强调需要扩大遗传测试的必要性. 早期遗传分析对于诊断POLR3A疾病至关重要,即使没有经典症状.

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