Mitochondrial diabetes is a topic covered in the Johns Hopkins Diabetes Guide.
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DEFINITION
- Mutations in the mitochondrial genome (mtDNA) can cause diabetes mellitus (DM).
- The distinguishing clinical feature of mitochondrial diabetes is association with other symptoms, including hearing impairment, neurological disorders, cardiac failure, and renal failure.
- These mutations can be large deletions, duplications, rearrangements, or point mutations.
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Last updated: October 6, 2015
Citation
* When formatting your citation, note that all book, journal, and database titles should be italicized* Article titles in AMA citation format should be in sentence-case
TY - ELEC
T1 - Mitochondrial diabetes
ID - 547094
A1 - Cooke,David,M.D.
AU - Mohamadi,Ali,M.D.
Y1 - 2015/10/06/
PB - Johns Hopkins Diabetes Guide
UR - https://www.hopkinsguides.com/hopkins/view/Johns_Hopkins_Diabetes_Guide/547094/all/Mitochondrial_diabetes
ER -