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Autosomal dominant polycystic kidney disease
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Autosomal dominant polycystic kidney disease

Clinical feature: 

Definition: ADPKD is an autosomal dominant disorder caused by mutations in one of the genes PKD1 or PKD2. It manifests in adults and one half of patient develop end stage renal disease.

Epidemiology: The prevalence is 1 one in 400 to one in 1000

Systematic link table: 

Cystic kidney disease
Autosomal dominant polycystic kidney disease
PKD1
PKD2
Autosomal recessive polycystic kidney and hepatic disease 1
PKHD1
Branchiootorenal dysplasia
MODY5 diabetes
HNF1B
Medullary cystic disease complex
Renal cysts and diabetes (RCAD)
HNF1B

Literature: