Clinical heterogeneity in two pedigrees with the 3243 bp tRNA(Leu(UUR)) mutation of mitochondrial DNA

Acta Neurol Scand. 1995 Jan;91(1):62-5. doi: 10.1111/j.1600-0404.1995.tb05845.x.

Abstract

We studied two pedigrees with a mutation at the nucleotide 3243 of mitochondrial DNA (mtDNA). The proband from the first pedigree had clinically defined MELAS plus maternally transmitted insulin-dependent diabetes mellitus (IDDM). The propositus of the other pedigree had exercise intolerance, lactic acidosis and ragged-red fibers (RRF). In the first pedigree, both the mother and the sister's proband harbored the point mutation in their muscle. The mother had 40% of mutant mitochondrial genomes and the sister 70%. In the second pedigree, the mutation was present in both muscle and blood from the proband as well as in blood from all other members studied. Proportion of mutant mtDNA was 90% in muscle and ranged from 40% to 90% in blood.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • DNA Primers
  • DNA, Mitochondrial / genetics*
  • Diabetes Mellitus, Type 1 / complications*
  • Electrophoresis, Agar Gel
  • Female
  • Humans
  • MELAS Syndrome / complications
  • Male
  • Middle Aged
  • Mitochondria, Muscle / genetics
  • Mutagenesis*
  • Pedigree*
  • Phenotype
  • Point Mutation
  • RNA, Transfer, Leu*

Substances

  • DNA Primers
  • DNA, Mitochondrial
  • RNA, Transfer, Leu