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Clinical variability of the cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in two siblings of a large family showing the same mutation

A 44-year-old Albanian male was consulted and diagnosed with dementia. His magnetic resonance imaging suggested diffuse white matter changes. The suspicion of cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) was raised, and a genetic analysis confi...

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Detalhes bibliográficos
Main Authors: Vyshka, Gentian, Kruja, Jera
Formato: Artigo
Idioma:Inglês
Publicado em: Dove Medical Press 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3794843/
https://ncbi.nlm.nih.gov/pubmed/24124395
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/IMCRJ.S51875
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