A Rare Case of Mitochondrial Neurogastrointestinal Encephalopathy

V. S. Hamsa; . Harivasudevan; . Jagadeeshwari; . Sundari

doi:10.9734/jpri/2021/v33i60A34534

Research Article Open access CC BY 4.0

A Rare Case of Mitochondrial Neurogastrointestinal Encephalopathy

V. S. Hamsa, . Harivasudevan, . Jagadeeshwari, . Sundari

Journal of Pharmaceutical Research International · pp. 694–696 · Published 20 Dec 2021

10.9734/jpri/2021/v33i60A34534

Abstract

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.

Mitochondrial neuro gastrointestinal encephalopathy leucoencephalopathy

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V. S. Hamsa, . Harivasudevan, . Jagadeeshwari, . Sundari (2021). A Rare Case of Mitochondrial Neurogastrointestinal Encephalopathy. Journal of Pharmaceutical Research International , 694–696. https://doi.org/10.9734/jpri/2021/v33i60A34534

Affiliations

V. S. Hamsa — Department of Paediatrics, Sree Balaji Medical College and Hospital, Chrompet, Chennai-600044, India.
. Harivasudevan — Department of Paediatrics, Sree Balaji Medical College and Hospital, Chrompet, Chennai-600044, India.
. Jagadeeshwari — Department of Paediatrics, Sree Balaji Medical College and Hospital, Chrompet, Chennai-600044, India.
. Sundari — Department of Paediatrics, Sree Balaji Medical College and Hospital, Chrompet, Chennai-600044, India.

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