伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(cerebral autosomal dominantart eriopathy with subcortical infarcts and leukoencephalopathy,CADASIL)是人类19p13上的Notch3基因突变所致的常染色体显性遗传的、非动脉硬...伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(cerebral autosomal dominantart eriopathy with subcortical infarcts and leukoencephalopathy,CADASIL)是人类19p13上的Notch3基因突变所致的常染色体显性遗传的、非动脉硬化或淀粉样变性的缺血性脑小动脉病^[1-2]。国内外影像学多限于MRI检查^[2-4],展开更多
文摘伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(cerebral autosomal dominantart eriopathy with subcortical infarcts and leukoencephalopathy,CADASIL)是人类19p13上的Notch3基因突变所致的常染色体显性遗传的、非动脉硬化或淀粉样变性的缺血性脑小动脉病^[1-2]。国内外影像学多限于MRI检查^[2-4],