Hepatic Nuclear Factor 1B Mutations
INFORMATION FOR PATIENTS

 

Hepatic Nuclear Factor 1B Mutations can cause renal cysts and diabetes syndrome, and in some cases this disease can present similarly to ADPKD or ADTKD.

 

What is HNF1B and how do HNF1B mutations affect people?

  • For an overview of HNF1B mutations, how these affect people and further information about the genetics of this – please click the following link;

 

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

If you would like to be part of a Disease Specific Research Group (DSRG) for Hepatic Nuclear Factor 1B Mutations, please contact the ARRK registry (arrkregistry1@gmail.com).

 

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 15th 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
  • Hepatic Nuclear Factor 1B Mutations
  • Haemolytic Uraemic Syndrome (Shiga Toxin Associated)
  • Hyperoxaluria
  • Membranoproliferative Glomerulonephritis (MPGN), Dense Deposit Disease (DDD) and C3 Glomerulopathy
  • Membranous Nephropathy
  • Nephronophthisis
  • Nephrotic Syndrome
  • Pregnancy and Chronic Kidney Disease
  • Tuberous Sclerosis
  • Vasculitis