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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Udgivet i:Front Neurol
Main Authors: Khan, Ayesha, Abedi, Vida, Li, Jiang, Malik, Muhammad T., Esch, Megan, Zand, Ramin
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2020
Fag:
Neurology
Online adgang: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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