KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease

Nephrology (Carlton). 2016 Aug;21(8):705-16. doi: 10.1111/nep.12658.
No abstract available

Keywords: autosomal-dominant polycystic kidney disease; clinical practice guidelines; genetic renal disease; management.

Publication types

  • Practice Guideline
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Algorithms
  • Combined Modality Therapy
  • Critical Pathways / standards
  • Diagnostic Imaging / standards*
  • Genetic Counseling / standards*
  • Genetic Markers
  • Genetic Predisposition to Disease
  • Genetic Testing / standards*
  • Humans
  • Middle Aged
  • Mutation
  • Nephrology / standards*
  • Phenotype
  • Polycystic Kidney, Autosomal Dominant / diagnosis*
  • Polycystic Kidney, Autosomal Dominant / diagnostic imaging
  • Polycystic Kidney, Autosomal Dominant / genetics
  • Polycystic Kidney, Autosomal Dominant / therapy*
  • Predictive Value of Tests
  • TRPP Cation Channels / genetics
  • Treatment Outcome
  • Young Adult

Substances

  • Genetic Markers
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein
  • polycystic kidney disease 2 protein