Autosomal recessive polycystic kidney disease (ARPKD)

J Nephrol. May-Jun 2003;16(3):453-8.

Abstract

Autosomal recessive polycystic kidney disease (ARPKD) is an important hereditary early childhood nephropathy. However, the clinical ARPKD spectrum is much more variable than is generally presumed. Presentation of ARPKD at a later age and survival into adulthood is well known. Diagnostic criteria, clinical course, differential diagnoses, genetics and molecular biology will be discussed along with the advantages and limitations of mutation detection in clinical practice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Diagnosis, Differential
  • Humans
  • Mutation
  • Phenotype
  • Polycystic Kidney, Autosomal Recessive / diagnosis*
  • Polycystic Kidney, Autosomal Recessive / genetics
  • Polycystic Kidney, Autosomal Recessive / pathology
  • Polycystic Kidney, Autosomal Recessive / physiopathology*
  • Prenatal Diagnosis
  • Receptors, Cell Surface / genetics
  • Survival Analysis

Substances

  • PKHD1 protein, human
  • Receptors, Cell Surface