Beware the thin, deaf 'type 2' diabetic: maternally inherited diabetes and deafness with systemic (mitochondrial) manifestations

Intern Med J. 2004 Aug;34(8):517-8. doi: 10.1111/j.1444-0903.2004.00659.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • Antioxidants / therapeutic use
  • Coenzymes
  • DNA Mutational Analysis
  • DNA, Mitochondrial / genetics*
  • Deafness / congenital*
  • Deafness / genetics
  • Diabetes Mellitus, Type 2 / congenital*
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / genetics
  • Female
  • Humans
  • Mitochondrial Diseases / complications*
  • Mitochondrial Diseases / diagnosis
  • Mitochondrial Diseases / genetics
  • Phenotype
  • Point Mutation
  • Ubiquinone / analogs & derivatives*
  • Ubiquinone / therapeutic use

Substances

  • Antioxidants
  • Coenzymes
  • DNA, Mitochondrial
  • Ubiquinone
  • coenzyme Q10