Open AccessA Rare Case of Mitochondrial Neurogastrointestinal Encephalopathy
Author(s) -
V Hamsa,
Harivasudevan,
Jagadeeshwari,
Sundari Sundari
Publication year - 2021
Publication title -
journal of pharmaceutical research international
Language(s) - English
Resource type - Journals
ISSN - 2456-9119
DOI - 10.9734/jpri/2021/v33i60a34534
Subject(s) - cachexia , encephalopathy , medicine , rare disease , pathology , biology , disease , cancer
Mitochondrial Neuro Gastrointestinal Encephalopathy (MNGIE) is rare genetic disorer. It is characteristic by progressive gastrointestinal dysmotility, cachexia, opthalmoplegia and leucoencephalopathy.We hereby report a case of MNGIE in a female.
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