Mitochondrial neurogastrointestinal encephalopathy: a case report

Mitochondrial neurogastrointestinal encephalopathy: a case report

Abstract Background Mitochondrial neurogastrointestinal encephalopathy (MNGIE) is an autosomal recessive disease associated with alterations in mitochondrial DNA (mtDNA). The typical age of onset of MNGIE is between the first and second decade of life. Diagnosis requires the presence of several key...

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Bibliographic Details
Main Authors: Ghazaleh Jamalipour Soufi, Ali Hekmatnia, Farzaneh Hekmatnia, Andrew Parviz Zarei, Farshad Riahi, Shamim Shafieyoon, Sara Azizollahi
Format: Article
Language:English
Published: SpringerOpen 2024-07-01
Series:The Egyptian Journal of Radiology and Nuclear Medicine
Subjects:
Mitochondrial neurogastrointestinal encephalopathy
Ophthalmoplegia
Demyelinating neuropathy
Online Access:https://doi.org/10.1186/s43055-024-01310-2

Internet

https://doi.org/10.1186/s43055-024-01310-2

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