Mitochondrial inheritance and disease

Lancet. 1978 Sep 23;2(8091):659-62. doi: 10.1016/s0140-6736(78)92764-2.

Abstract

Spontaneously occurring variants of the D.N.A. content of mitochondria may be responsible for human disease. Among the prime candidates for such a mitochondrial aetiology are certain drug-induced blood dyscrasias, particularly that due to chloramphenicol. Because mitochondria are generally inherited from the female parent, such disorders should be clustered among matroclinally related individuals. The clinical manifestations of such diseases are a function of the manner in which mitochondria are allocated to somatic cells and tissues during development.

MeSH terms

  • Adult
  • Child
  • Chloramphenicol / toxicity*
  • DNA, Mitochondrial / genetics*
  • Drug Hypersensitivity / genetics*
  • Female
  • Genetic Carrier Screening
  • Hematologic Diseases / chemically induced*
  • Hematologic Diseases / genetics
  • Hematopoietic Stem Cells / cytology
  • Humans
  • Male
  • Mitochondria / drug effects
  • Pedigree
  • Sex Factors

Substances

  • DNA, Mitochondrial
  • Chloramphenicol