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Adult-onset vanishing white matter disease with the EIF2B2 gene mutation presenting as menometrorrhagia
BACKGROUND: Vanishing white matter disease (VWMD) is one of the most prevalent inherited leukoencephalopathies, which generally presents in childhood as a progressive disorder while less beginning in adulthood. The present report describes the clinical, neuroimaging, and genetic findings of a female...
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| Pubblicato in: | BMC Neurol |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6704498/ https://ncbi.nlm.nih.gov/pubmed/31438897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-019-1429-9 |
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