Infantile Alexander Disease with Late Onset Infantile Spasms and Hypsarrhythmia

Alexander disease (AxD) is a rare autosomal dominant leukodystrophy with three clinical subtypes: infantile, juvenile and adult. Forms differ by age of symptoms occurrence and the clinical presentation. Although recent data suggest considering only two subtypes: type I (infantile onset with lesions...

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Detalles Bibliográficos
Autores principales: Paprocka, J, Rzepka-Migut, B, Rzepka, N, Jezela-Stanek, A, Morava, E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956636/
https://www.ncbi.nlm.nih.gov/pubmed/31942421
http://dx.doi.org/10.2478/bjmg-2019-0017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956636/
https://www.ncbi.nlm.nih.gov/pubmed/31942421
http://dx.doi.org/10.2478/bjmg-2019-0017

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