Bartter Syndrome
INFORMATION FOR HEALTH PROFESSIONALS

 

Bartter Syndrome is a group of rare autosomal recessive genetic disorders that result in specific defects in kidney function.

 

Link to Gene Reviews or Guidelines

 

More detailed Information for Health Professionals will be available on the ARRK website in the near future.

If you would like to form or be part of a Disease Specific Research Group (DSRG) for Bartter Syndrome, please contact the ARRK registry (arrkregistry1@gmail.com) or Dr Hugh McCarthy (hugh.mccarthy@health.nsw.gov.au).

 

The resources on this page provide information for healthcare professionals. If you have questions about a medical condition or health related issue, please consult your medical doctor or a healthcare professional.

 

This page was last updated on 24th Oct, 2018.

  • Alport Syndrome
  • Atypical Haemolytic Uraemic Syndrome (aHUS)
  • Autosomal Dominant Polycystic Kidney Disease (ADPKD)
  • Autosomal Dominant Tubulointerstitial Kidney Disease (ADTKD)
  • Autosomal Recessive Polycystic Kidney Disease (ARPKD)
  • Bartter Syndrome
  • Calciphylaxis
  • Cystinosis
  • Cystinuria
  • Dent Disease and Lowe Syndrome
  • Gitelman Syndrome
  • Haemolytic Uraemic Syndrome (Shiga Toxin Associated)
  • Hepatic Nuclear Factor 1B Mutations
  • Hyperoxaluria
  • Membranoproliferative Glomerulonephritis (MPGN), Dense Deposit Disease (DDD) and C3 Glomerulopathy
  • Membranous Nephropathy
  • Nephronophthisis
  • Nephrotic Syndrome
  • Pregnancy and Chronic Kidney Disease
  • Tuberous Sclerosis
  • Vasculitis