Autosomal dominant polycystic kidney disease in the 1980's

Clin Genet. 1989 Nov;36(5):320-5. doi: 10.1111/j.1399-0004.1989.tb03204.x.

Abstract

Since it is one of the commonest hereditary diseases, causing serious illness in adulthood, autosomal dominant polycystic kidney disease (ADPKD) is a problem for both the affected families and for the health economy of the society. The current management of ADPKD is reviewed with emphasis on the development of predictive DNA analyses, the recently discovered genetic heterogeneity, and ethical perspectives. Insurance aspects are discussed, and the need for access to selective reproductive prevention as well as for improvement of conventional therapeutic measures is stressed.

Publication types

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

MeSH terms

  • Chromosome Mapping
  • Ethics, Medical
  • Genes, Dominant*
  • Genetic Counseling
  • Genetic Markers
  • Humans
  • Pedigree
  • Polycystic Kidney Diseases / diagnosis
  • Polycystic Kidney Diseases / genetics*
  • Polycystic Kidney Diseases / prevention & control
  • Prognosis

Substances

  • Genetic Markers