Hereditary Kidney Diseases

Hereditary kidney disorders represent significant risk for the development of end stage renal disease (ESRD). Most of them are recognized in childhood, or prenatal particularly those phenotypically expressed as anomalies on ultrasound examination (US) during pregnancy. Some kidney diseases result from genetic factors. Polycystic Kidney Disease (PKD), for example, is a genetic disorder in which many cysts grow in the kidneys. PKD cysts will slowly switch a lot of the mass of the kidneys, decreasing urinary organ perform and resulting in failure. Some urinary organ complications might show up even before birth. Examples contain autosomal recessive PKD (ARPKD) a rare form of PKD, and other developing problems that interfere with the normal formation of the nephrons. The signs of kidney disease in children vary.

  • Polycystic kidney disease
  • Medullary sponge kidney
  • Bartter syndrome
  • Alport syndrome
  • Horseshoe kidney
  • Nephronophthisis
  • Tuberous sclerosis

Related Conference of Hereditary Kidney Diseases

August 20-21, 2020

16th World Nephrology Conference

Prague, Czech Republic
September 07-08, 2020

22nd World Nephrologists Summit

Tokyo, Japan
September 14-15, 2020

17th Asia Pacific Nephrology Conference

Osaka, Japan
September 16-17, 2020

15th Nephrology,Renal Medicine & Renal Care

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October 12-13, 2020

24th European Nephrology Conference

Zurich, Switzerland
October 26-27, 2020

3rd International Conference on Nephrology

Dubai, UAE
November 09-10, 2020

International Conference on  Urology and Andrology

Bangkok, Thailand
November 23-24, 2020

World Congress and Expo on Nephrology

Hanoi, Vietnam

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