DAC NO.: HDAC003291
DAC name: inherited metabolic disorder
Contact person: Zhang Xiaomei
URL: https://pubmed.ncbi.nlm.nih.gov/32847542/
Description: Mitochondrial diabetes is a rare monogenic diabetes, and the most common mutation type is m.3243A>G. The clinical features of mitochondrial diabetes are mainly diabetes, deafness, vision loss and other system abnormalities. Here, the NMDAS was used to comprehensively manage a case of new-onset mitochondrial diabetes to deeply understand the characteristics of the disease and improve our clinical diagnosis and treatment level.
