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  • Mitochondrial disease: an uncommon but important cause of diabetes . . .
    Mitochondrial diseases are rare, heterogeneous conditions caused by mutations in either the mitochondrial or nuclear DNA and can present with a variety of clinical symptoms Mitochondrial mutation is more common and is transmitted through maternal inheritance
  • Mitochondrial Diabetes: More Than Just Hyperglycemia
    Here, we report on a genetically proven mitochondrial A3243G mutation–related syndromic diabetes in a young patient whose mitochondrial disease–related multisystem symptomatology slowly evolved over the course of a decade
  • Can very low HbA1c be a sign of a health problem?
    Additionally, if the low HbA1c is due to an underlying condition like hemolytic anemia or liver disease, failing to identify and treat these conditions can lead to serious complications Diagnostic Approach for Very Low HbA1c When evaluating very low HbA1c, healthcare providers typically take a comprehensive approach:
  • Mitochondrial Diseases: Causes, Symptoms Treatment - Cleveland Clinic
    There are many types of mitochondrial diseases Some of the most common include: Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome Leber hereditary optic neuropathy (LHON) Leigh syndrome Kearns-Sayre syndrome (KSS) Myoclonic epilepsy and ragged-red fiber disease (MERRF) How common is mitochondrial disease?
  • Diabetes Mellitus in Adult Mitochondrial Disease: Screening and Initial . . .
    Diabetes mellitus is a common endocrine feature of patients with mitochondrial disease, predominantly due to its association with the m 3243A>G mutation, the most common heteroplasmic mtDNA mutation associated with human disease





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