Case report: Alexander's disease with “head drop” as the main symptom and literature review

Alexander's disease (AxD) is a rare autosomal dominant hereditary disorder that is caused by the mutations in the GFAP gene, which encodes the glial fibrillary acidic protein (GFAP). This neurogenerative disease has many clinical manifestations, and the onset of disease spans a wide range of ag...

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Detalles Bibliográficos
Autores principales: Yuan, Yujun, Wu, Qiong, Huo, Liang, Wang, Hua, Liu, Xueyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807021/
https://www.ncbi.nlm.nih.gov/pubmed/36601294
http://dx.doi.org/10.3389/fneur.2022.1002527

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807021/
https://www.ncbi.nlm.nih.gov/pubmed/36601294
http://dx.doi.org/10.3389/fneur.2022.1002527

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