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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...
Autores principales: | Bahrami, Sima, Arshi, Saba, Nabavi, Mohammad, Bemanian, Mohammad Hassan, Fallahpour, Morteza, Rezaeifar, Afshin, Shokri, Sima |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
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 |
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