Publication: Mitochondrial Diabetes A Rare Case
Date
2017
Article Type
Case Report
Journal Title
Journal ISSN
ISSN 1990-7974 eISSN 1990-7982
Volume Title
Pages
Pages: 290 - 292
Publisher
Nepal Paediatric Society (JNPS)
Abstract
Abstract:
A 25 years female diagnosed and confirmed mitochondrial by gene analysis mutation DNA 3243(A-G). CQ10 was useful for the resolution of clinical symptoms, and metformin should be avoided in mito-chondrial diabetes.
Description
Arun Kumar Singh
B.P.Koirala Institute of Health Sciences
Aoki Msasko
Department of Paediatrics, Nihon University Hospital,Tokyo
Midori Miyata
Department of Paediatrics, Nihon University Hospital,Tokyo
Yasuke Mine
Department of Paediatrics, Nihon University Hospital,Tokyo
Junichi Suzuki
Department of Paediatrics, Nihon University Hospital,Tokyo
Tatsuhiko Urakami
Department of Paediatrics, Nihon University Hospital,Tokyo
Keywords
Mitochondrial diabetes, Metformin, Wolff-Parkinson-White (WPW) syndrome
Identifier
https://doi.org/10.3126/jnps.v37i3.18765