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

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