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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Detalles Bibliográficos
Autores principales: Khan, Ayesha, Abedi, Vida, Li, Jiang, Malik, Muhammad T., Esch, Megan, Zand, Ramin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
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

Internet

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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