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CADASIL vs. Multiple Sclerosis: Is It Misdiagnosis or Concomitant? A Case Series
Introduction: Cerebral autosomal dominant arteriopathy and subcortical infarct leukoencephalopathy (CADASIL) is the most common form of hereditary stroke caused by a mutation in the NOTCH3 gene located on the short arm of chromosome 19. A small number of published reports describe CADASIL patients w...
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| Publicado no: | Front Neurol |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7500095/ https://ncbi.nlm.nih.gov/pubmed/33013620 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.00860 |
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