Genetic Kidney Disease

Polycystic Kidney Disease (PKD) is result from hereditary factors. In polycystic kidney disease number of cysts develops in the kidney, these cysts gradually replace the mass of kidney. Impairing kidney function and leading to renal failure.

  • Polycystic Kidney Disease
  • Autosomal Dominant Polycystic Kidney Disease
  • Cystic Diseases of the Kidney
  • Autosomal Recessive Polycystic Kidney Disease
  • Alport Syndrome
  • Medullary Cystic Kidney Disease
  • Nephronophthisis
  • Bartter Syndrome
  • Congenital Nephrotic Syndrome
  • Ciliopathy
  • Von Hippel–Lindau Disease
  • Tuberous Sclerosis
  • Renal Agenesis
  • Atypical Hemolytic Uremic Syndrome
  • Cystinuria
  • Hypercalciuria
  • Fabry Disease
  • Gitelman Syndrome
  • Cystinosis
  • Branchiootorenal Syndrome
  • Papillorenal Syndrome
  • Oculocerebrorenal Syndrome
  • Senior-Løken Syndrome
  • Meckel-Gruber Syndrome
  • Tubulopathy
  • Fraser Syndrome
  • Primary Hyperoxaluria
  • Bardet-Biedl Syndrome
  • Mineral and Bone Disorder in Chronic Kidney Disease

Related Conference of Genetic Kidney Disease

May 14-15, 2018

19th Global Nephrologists Annual Meeting

Rome, Italy
June 8-9, 2018

3rd Annual Kidney Congress

Baltimore, USA
June 8-9, 2018

16th Annual Dialysis & Renal Medicine Conference

Baltimore, USA
June 28-29, 2018

20th World Kidney Congress

Berlin, Germany
October 15-16, 2018

22nd European Nephrology Conference

Warsaw, Poland

Genetic Kidney Disease Conference Speakers

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