A Rare Case of Mitochondrial Neurogastrointestinal Encephalopathy

Hamsa, V. S. and Harivasudevan, . and Jagadeeshwari, . and Sundari, . (2021) A Rare Case of Mitochondrial Neurogastrointestinal Encephalopathy. Journal of Pharmaceutical Research International, 33 (60A). pp. 694-696. ISSN 2456-9119

[thumbnail of 5136-Article Text-7246-1-10-20221006.pdf]

Text
5136-Article Text-7246-1-10-20221006.pdf - Published Version
Download (364kB)

Official URL: https://doi.org/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.

Item Type:	Article
Subjects:	STM Archives > Medical Science
Depositing User:	Unnamed user with email support@stmarchives.com
Date Deposited:	07 Apr 2023 08:13
Last Modified:	29 Jun 2024 12:24
URI:	http://science.scholarsacademic.com/id/eprint/138

Actions (login required)

: View Item