Identification of mtDNA mutation in a pedigree with gestational diabetes, deafness, Wolff-Parkinson-White syndrome and placenta accreta

Hum Hered. 2001;51(1-2):114-6. doi: 10.1159/000022950.

Abstract

Mitochondrial DNA (mtDNA) defects are associated with a number of human disorders. Although many occur sporadically, maternal transmission is the hallmark of diseases due to mtDNA point mutations. The same mutation may manifest strikingly different phenotypes; for example, the A to G substitution at np 3243 was first reported in patients with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (the MELAS syndrome), but is also found in patients with diabetes and deafness. Here we present a case of gestational diabetes, deafness, premature greying, placenta accreta and Wolff-Parkinson-White (WPW) syndrome associated with a mtDNA mutation. Although this is the first report of such an association, study of 27 other patients with WPW syndrome failed to confirm that this mtDNA mutation is a common cause of such pre-excitation disorders.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • DNA, Mitochondrial / genetics*
  • Deafness / complications
  • Deafness / genetics*
  • Diabetes, Gestational / complications
  • Diabetes, Gestational / genetics*
  • Female
  • Humans
  • Pedigree
  • Placenta Accreta / complications
  • Placenta Accreta / genetics*
  • Point Mutation*
  • Polymerase Chain Reaction
  • Pregnancy
  • Wolff-Parkinson-White Syndrome / complications
  • Wolff-Parkinson-White Syndrome / genetics*

Substances

  • DNA, Mitochondrial