Mitochondrial Diabetes A Rare Case

Authors

  • 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

DOI:

https://doi.org/10.3126/jnps.v37i3.18765

Keywords:

Mitochondrial diabetes, Metformin, Wolff-Parkinson-White (WPW) syndrome

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.

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Author Biography

Arun Kumar Singh, B.P.Koirala Institute of Health Sciences

Paedatrician. Fellowship in diabetics and endocrinologist 

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Published

2018-06-07

How to Cite

Singh, A. K., Msasko, A., Miyata, M., Mine, Y., Suzuki, J., & Urakami, T. (2018). Mitochondrial Diabetes A Rare Case. Journal of Nepal Paediatric Society, 37(3), 290–292. https://doi.org/10.3126/jnps.v37i3.18765

Issue

Vol. 37 No. 3 (2017)

Section

Case Reports

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