Inflammatory-like presentation of CADASIL: a diagnostic challenge

BACKGROUND: CADASIL is an autosomal dominant genetic leukoencephalopathy linked to mutations in the Notch3 gene. In rare cases, widespread brain lesions on T2 MRI mimicking multiple sclerosis are observed. From a national registry of 268 patients with adult-onset leukodystrophy, we identified two pa...

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Detalles Bibliográficos
Autores principales: Collongues, Nicolas, Derache, Nathalie, Blanc, Frédéric, Labauge, Pierre, de Seze, Jérôme, Defer, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488471/
https://www.ncbi.nlm.nih.gov/pubmed/22905984
http://dx.doi.org/10.1186/1471-2377-12-78

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488471/
https://www.ncbi.nlm.nih.gov/pubmed/22905984
http://dx.doi.org/10.1186/1471-2377-12-78

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