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 05-06, 2025
7th International Conference on Clinical Immunology, Neuropharmacology and Drug Development
Rome, Italy
Genetic Kidney Disease Conference Speakers
Recommended Sessions
- Acute Kidney Injury
- Chronic Kidney Disease
- Complications during Dialysis
- Dialysis
- Fluid, Electrolytes, Acid-Base Disorders
- Genetic Kidney Disease
- Glomerular Disorders
- Hemodialysis
- Home Dialysis
- Kidney Cancer
- Kidney Stones
- Kidney Transplantation
- Mineral and Bone Disorders
- Nursing & Health Care
- Pediatric Renal Care
- Peritoneal Dialysis
- Renal Nutrition
- Renal physiology
- Urology
- Vascular Access
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