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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...
Autores principales: | Khan, Ayesha, Abedi, Vida, Li, Jiang, Malik, Muhammad T., Esch, Megan, Zand, Ramin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500095/ https://www.ncbi.nlm.nih.gov/pubmed/33013620 http://dx.doi.org/10.3389/fneur.2020.00860 |
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