Atypical clinical cases of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
C Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary CNS disease with autosomal dominant inheritance caused by NOTCH3 gene mutations. In classic cases, CADASIL manifests with headaches, repeated cerebrovascular disorders, and progr...
| Những tác giả chính: | , , , , , |
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| Định dạng: | Bài viết |
| Ngôn ngữ: | English |
| Được phát hành: |
Research Center of Neurology
2017-05-01
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| Loạt: | Анналы клинической и экспериментальной неврологии |
| Những chủ đề: | |
| Truy cập trực tuyến: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/462/358 |