Simultaneous adult polycystic kidney disease and Alport syndrome

Nephrology (Carlton). 2016 Aug;21(8):722-3. doi: 10.1111/nep.12661.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Child, Preschool
  • Codon, Nonsense
  • Collagen Type IV / genetics
  • DNA Mutational Analysis
  • Disease Progression
  • Genetic Predisposition to Disease
  • Heredity
  • Humans
  • Kidney Failure, Chronic / diagnosis
  • Kidney Failure, Chronic / etiology
  • Kidney Failure, Chronic / surgery
  • Kidney Transplantation
  • Magnetic Resonance Imaging
  • Male
  • Mutation, Missense
  • Nephrectomy
  • Nephritis, Hereditary / complications*
  • Nephritis, Hereditary / diagnosis
  • Nephritis, Hereditary / genetics
  • Pedigree
  • Phenotype
  • Polycystic Kidney, Autosomal Dominant / complications*
  • Polycystic Kidney, Autosomal Dominant / diagnosis
  • Polycystic Kidney, Autosomal Dominant / genetics
  • Polycystic Kidney, Autosomal Dominant / surgery
  • TRPP Cation Channels / genetics

Substances

  • COL4A5 protein, human
  • Codon, Nonsense
  • Collagen Type IV
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein