Progressive multifocal leukoencephalopathy in a patient with novel mutation in the RAC2 gene: a case report

BACKGROUND: Progressive multifocal leukoencephalopathy is a rare demyelinating disease that is often secondary to lytic destruction of oligodendrocytes and, to a lesser extent, to astrocytes’ response to human neurotrophic John Cunningham polyomavirus. Any underlying congenital disorder of primary o...

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Detalles Bibliográficos
Autores principales: Bahrami, Sima, Arshi, Saba, Nabavi, Mohammad, Bemanian, Mohammad Hassan, Fallahpour, Morteza, Rezaeifar, Afshin, Shokri, Sima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188039/
https://www.ncbi.nlm.nih.gov/pubmed/35689244
http://dx.doi.org/10.1186/s13256-022-03333-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188039/
https://www.ncbi.nlm.nih.gov/pubmed/35689244
http://dx.doi.org/10.1186/s13256-022-03333-7

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