Late-Onset Melas with Midd: An Uncommon Age of Presentation
ABSTRACT: Objective: Maternally inherited diabetes and deafness (MIDD) is a rare form of diabetes caused by a mutation in mitochondrial DNA, usually a point mutation at position 3243 in the leucine tRNA gene. This same mutation can cause a rare but severe syndrome called mitochondrial encephalomyopa...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2018-05-01
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| Series: | AACE Clinical Case Reports |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2376060520304971 |