Mitochondrial Neurogastrointestinal Encephalopathy Disease: A Rare Disease Diagnosed in Siblings with Double Vision

Mitochondrial neurogastrointestinal encephalopathy disease (MNGIE) is a rare autosomal recessive condition characterized by gastrointestinal dysmotility, external ophthalmoplegia, leukoencephalopathy, and sensorimotor neuropathy. A 31-year-old man was referred for a 1-year history of horizontal dipl...

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Detalles Bibliográficos
Autores principales: Farahvash, Armin, Kassardjian, Charles D., Micieli, Jonathan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077549/
https://www.ncbi.nlm.nih.gov/pubmed/33976678
http://dx.doi.org/10.1159/000514098

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077549/
https://www.ncbi.nlm.nih.gov/pubmed/33976678
http://dx.doi.org/10.1159/000514098

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