A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes

J Med Genet. 1997 Jul;34(7):587-9. doi: 10.1136/jmg.34.7.587.

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is a genetically heterogeneous disease. Most families show positive linkage to polymorphic markers around the PKD1 (16p13.3) or PKD2 (4q21-23) loci. The PKD1 and PKD2 genes have been cloned and mutations defined in a number of patients. Several clinical studies have described a milder phenotype for PKD2 patients. More recently, evidence for a third genetic locus has been found in one Portuguese, one French-Canadian, and one Italian family. We identified a Spanish family with negative linkage to the PKD1 and the PKD2 loci. This family showed a very mild clinical phenotype compared to the other forms of ADPKD, including the non-PKD1/non-PKD2 families previously described.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 16*
  • Chromosomes, Human, Pair 4*
  • Cloning, Molecular
  • Female
  • Genetic Heterogeneity
  • Genetic Linkage*
  • Humans
  • Male
  • Membrane Proteins / genetics
  • Microsatellite Repeats
  • Mutation
  • Pedigree
  • Polycystic Kidney, Autosomal Dominant / genetics*
  • Polycystic Kidney, Autosomal Dominant / physiopathology
  • Polymorphism, Restriction Fragment Length
  • Proteins / genetics
  • TRPP Cation Channels

Substances

  • Membrane Proteins
  • Proteins
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein
  • polycystic kidney disease 2 protein