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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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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3488471/ https://ncbi.nlm.nih.gov/pubmed/22905984 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-12-78 |
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