Infantile-onset Alexander disease in a child with long-term follow-up by serial magnetic resonance imaging: a case report

INTRODUCTION: Alexander disease is a rare disorder resulting from a glial fibrillary acidic protein gene mutation which causes progressive degeneration of white matter. With the usual poor prognosis, there are few case reports with long-term follow-up. We report the five-year clinical course of Alex...

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Detalles Bibliográficos
Autores principales: Nishibayashi, Fumiko, Kawashima, Miho, Katada, Yoshiaki, Murakami, Nobuyuki, Nozaki, Miwako
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231460/
https://www.ncbi.nlm.nih.gov/pubmed/23890466
http://dx.doi.org/10.1186/1752-1947-7-194

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231460/
https://www.ncbi.nlm.nih.gov/pubmed/23890466
http://dx.doi.org/10.1186/1752-1947-7-194

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