RecruitingNCT03059420
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies
Sponsor
Boston Children's Hospital
Enrollment
20,000 participants
Start Date
Feb 1, 2004
Study Type
OBSERVATIONAL
Conditions
Facial PalsyCongenital Fibrosis of Extraocular MusclesDuane Retraction SyndromeDuane Radial Ray SyndromeMobius SyndromeBrown SyndromeMarcus Gunn SyndromeStrabismus CongenitalHorizontal Gaze PalsyHorizontal Gaze Palsy With Progressive ScoliosisFacial Paresis, Hereditary, CongenitalThird Nerve PalsyFourth Nerve PalsySixth Nerve PalsySynkinesisOcular Motility DisordersLevator-Medial Rectus SynkinesisAthabaskan Brainstem DysgenesisTongue ParalysisNinth Nerve DisorderFifth Nerve PalsySeventh Nerve PalsyEleventh Nerve DisorderTwelfth Nerve DisorderVagus Nerve ParalysisMoebius Sequence
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
Min Age: 1 Day
Plain Language Summary
Simplified for easier understanding
This clinical trial is studying a new treatment for people with athabaskan brainstem dysgenesis, brown syndrome, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 1 Day and older.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT03059420
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