A Case of Adult-Onset Alexander Disease Featuring Severe Atrophy of the Medulla Oblongata and Upper Cervical Cord on Magnetic Resonance Imaging

Adult-onset Alexander disease (AOAD) has been increasingly recognized since the identification of the glial fibrillary acidic protein gene mutation in 2001. We report on a 56-year-old man who was genetically confirmed as AOAD with the glial fibrillary acidic protein mutation of p.M74T. He developed...

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Detalles Bibliográficos
Autores principales: Yonezu, Tadahiro, Ito, Shoichi, Kanai, Kazuaki, Masuda, Saeko, Shibuya, Kazumoto, Kuwabara, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2012
Materias:
Published online: November, 2012
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506048/
https://www.ncbi.nlm.nih.gov/pubmed/23185175
http://dx.doi.org/10.1159/000345303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506048/
https://www.ncbi.nlm.nih.gov/pubmed/23185175
http://dx.doi.org/10.1159/000345303

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