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

June 13-14, 2024

9th World Kidney Congress

Barcelona, Spain
July 25-26, 2024

28th European Nephrology Conference

Frankfurt, Germany
October 03-04, 2024

22nd International Conference on Nephrology, Urology and Therapeutics

Singapore City, Singapore

Genetic Kidney Disease Conference Speakers

    Recommended Sessions

    Related Journals

    Are you interested in