Disease Specific Information
INFORMATION FOR PATIENTS

 

A list of Rare and Genetic Kidney Diseases is shown below, with links to further information about each specific disease.

 

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

If you have a rare or genetic kidney disease listed below and would like to be part of the ARRK registry, please speak to your kidney doctor.

If you would like to be part of a Disease Specific Research Group (DSRG) for any of the diseases listed below, please contact the ARRK registry (arrkregistry1@gmail.com).

 

Alport Syndrome

Atypical Haemolytic Uraemic Syndrome (aHUS)

Autosomal Dominant Polycytic 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

 

The resources on this site should not be used as a replacement for care or advice from your medical doctor. 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 3rd Sept, 2018.