Genetic identification and genotype-phenotype study in inherited cystic kidney disease
Not Applicable
Recruiting
- Conditions
- Congenital malformations, deformations and chromosomal abnormalities
- Registration Number
- KCT0005580
- Lead Sponsor
- Seoul National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 1200
Inclusion Criteria
Patients with 3 or more cysts in kidneys
-Typical ADPKD
-Atypical ADPKD
-Tuberous sclerosis complex
-von Hippel-Lindau disease
-Autosomal dominant tubulo-interstitial kidney disease
-Autosomal recessive polycystic kidney disease
-Nephronophthisis
Exclusion Criteria
Those who are not able to give informed consent or pregnant will be excluded from enrollment. The cases of simple renal cyst and acquired cystic kidney disease which involve cyst formation as the result of renal failure will also be excluded from this study.
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ovel cystogenesis-related genes
- Secondary Outcome Measures
Name Time Method Genes related to the severity of disease