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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2013
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| Materias: | |
| 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 |