Leukoencephalopathy with vanishing white matter disease: a case report study

Vanishing white matter (VWM) is a neurological disorder that has an autosomal recessive mode of inheritance. VWM is caused due to a mutation in in any of the five genes of eukaryotic translation initiation factor 2B (eIF2B). The etiology is unknown. CASE PRESENTATION: The authors report two cases of...

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Detalles Bibliográficos
Autores principales: Kami, Atefe, Langari, Alale, Gharib, Mohammad H., Ghelichi-Ghojogh, Mousa, Hosseini, Parmis S., Hosseini, Seyed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406083/
https://www.ncbi.nlm.nih.gov/pubmed/37554904
http://dx.doi.org/10.1097/MS9.0000000000001017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406083/
https://www.ncbi.nlm.nih.gov/pubmed/37554904
http://dx.doi.org/10.1097/MS9.0000000000001017

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