Phenotype Correlates Genotype of Inherited Retina Dystrophies
Status: Unknown
Location: See location...
Intervention Type: Diagnostic test, Procedure
Study Type: Observational
SUMMARY
Patients with retina dystrophies (retinitis pigmentosa, cone\>rods dystrophies, Usher and syndromic) will be correlated with genotype and validate inheritance mode by segregation analysis.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 14 days
Maximum Age: 90
Healthy Volunteers: t
View:
• Diagnosis of inherited retina dystrophy or retinitis pigmentosa
• Must be able to perform all study tests.
• Must be able to visit every year.
Locations
Other Locations
Mexico
Retina and Genomics Institute
RECRUITING
Mérida
Contact Information
Primary
A Villanueva, MD
dr.villanueva@mejoravisionmd.com
019992233623
Backup
Gelly Cuevas, MS
research.biobanks@mejoravisionmd.com
+521 (999) 4060506
Time Frame
Start Date: 2009-08
Completion Date: 2025-09-30
Participants
Target number of participants: 17000
Treatments
Retinitis pigmentosa
Any type of retina dystrophy with pigment / retinitis pigmentosa
Usher Syndrome
Retina dystrophy or retinitis pigmentosa associated with audition problems
Cone>rod syndromes
Retina dystrophy diagnosed or started in central vision.
Retinitis pigmentosa sx
Retinitis pigmentosa with any type of other features
Related Therapeutic Areas
Sponsors
Leads: MejoraVisionMD
Collaborators: Maisonneuve-Rosemont Hospital, Retina and Genomics Institute