A Rare Case of Mitochondrial Neurogastrointestinal Encephalopathy
Author(s): Hamsa VS*, Harivasudevan, Jagadeeshwari and Sundari
Abstract
Mitochondrial Neuro Gastrointestinal Encephalopathy (MNGIE) is rare genetic disorder. It is characteristic by progressive gastrointestinal dysmotility, cachexia, opthalmoplegia and leucoencephalopathy. We hereby report a case of MNGIE in a female.