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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wei, Cuibai, Qin, Qi, Chen, Fei, Zhou, Aihong, Wang, Fen, Zuo, Xiumei, Chen, Rong, Lyu, Jihui, Jia, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704498/
https://www.ncbi.nlm.nih.gov/pubmed/31438897
http://dx.doi.org/10.1186/s12883-019-1429-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704498/
https://www.ncbi.nlm.nih.gov/pubmed/31438897
http://dx.doi.org/10.1186/s12883-019-1429-9

Ejemplares similares