Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies
Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY
The purpose of this study is to identify genes associated with impaired development and function of the cranial nerves and brainstem, which may result in misalignment of the eyes (strabismus) and related conditions.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 1 day
View:
• The Engle Lab is very interested in enrolling individuals with congenital conditions related to eye movement, cranial nerve and brainstem-based dysfunction, often broadly referred to as congenital cranial dysinnervation disorders (CCDDs).
Locations
United States
Massachusetts
Boston Children's Hospital
RECRUITING
Boston
Contact Information
Primary
Brenda J Barry, MS
brenda.barry2@childrens.harvard.edu
617-919-2168
Backup
Engle Admin
engle.admin@childrens.harvard.edu
617-919-4030
Time Frame
Start Date: 2004-02-01
Estimated Completion Date: 2027-01
Participants
Target number of participants: 20000
Related Therapeutic Areas
Sponsors
Collaborators: Howard Hughes Medical Institute, National Eye Institute (NEI)
Leads: Boston Children's Hospital