CADASIL syndrome and demyelination: dual pathology? (a case report)
CADASIL syndrome (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is a rare hereditary disease affecting the brain associated with a mutation of the NOTCH3 gene on the 19th chromosome. Additional difficulties arise with the comorbidity of CADASIL syndrome...
| Main Authors: | , |
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| Format: | Article |
| Language: | Russian |
| Published: |
ABV-press
2022-01-01
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| Series: | Русский журнал детской неврологии |
| Subjects: | |
| Online Access: | https://rjdn.abvpress.ru/jour/article/view/389 |