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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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Detalhes bibliográficos
Publicado no:BMC Neurol
Main Authors: Wei, Cuibai, Qin, Qi, Chen, Fei, Zhou, Aihong, Wang, Fen, Zuo, Xiumei, Chen, Rong, Lyu, Jihui, Jia, Jianping
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Acesso em linha: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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