Older adult-onset Alexander disease with atypical clinicoradiological features: a case report

Alexander disease (AxD) is a rare autosomal dominant astrogliopathy caused by mutations in the gene encoding for glial fibrillary acidic protein. AxD is divided into two clinical subtypes: type I and type II AxD. Type II AxD usually manifests bulbospinal symptoms and occurs in the second decade of l...

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Detalles Bibliográficos
Autores principales: Kang, You-Ri, Nam, Tai-Seung, Kim, Jae-Myung, Kang, Kyung Wook, Lee, Seung-Han, Choi, Seong-Min, Kim, Myeong-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10310951/
https://www.ncbi.nlm.nih.gov/pubmed/37396762
http://dx.doi.org/10.3389/fneur.2023.1139047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10310951/
https://www.ncbi.nlm.nih.gov/pubmed/37396762
http://dx.doi.org/10.3389/fneur.2023.1139047

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