Hepatic Nuclear Factor 1B Mutations
INFORMATION FOR HEALTH PROFESSIONALS

 

Hepatic Nuclear Factor 1B Mutations cause an autosomal dominant disease that causes renal cysts and diabetes (RCAD) syndrome.

 

Link to Reviews or Guidelines

 

 Further Information

  • Verhave, J.H. et al. (2016). Hepatocyte Nuclear Factor 1β–Associated Kidney Disease: More than Renal Cysts and Diabetes. JASN 27 (2); 345-353.
  • Clissold R.L. et al. (2015). HNF1B-associated renal and extra-renal disease–an expanding clinical spectrum. Nature Reviews Nephrology 11 (2); 102-112.

 

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 Hepatic Nuclear Factor 1B Mutations, 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.

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  • 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