Genetic testing for Japanese retinitis pigmentosa and related diseases
Not Applicable
Recruiting
- Conditions
- Inherited chorioretinal dystrophies: retinitis pigmentosa, Leber congenital amaurosis, Stargardt Disease, Bardet-Biedl syndrome, Usher syndrome, Joubert syndrome, Refsum disease, Bietti crystalline corneoretinal dystrophy, X-linked juvenile retinoschisis, occult macular dystrophy, congenital stationary night blindness, choroideremia, Oguchi disease, fundus albipunctatus, and other chorioretinal dystrophies
- Registration Number
- JPRN-UMIN000018565
- Lead Sponsor
- Center for Genomic Medicine, Kyoto University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 1000
Inclusion Criteria
Not provided
Exclusion Criteria
Non Japanese genetic background supposed
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method molecular diagnosis (positive or negative findings)
- Secondary Outcome Measures
Name Time Method