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Genetic Studies of Strabismus, Nystagmus, and Associated Disorders

Strabismus Clinical Trial

Official title:
Genetic Studies of Strabismus, Nystagmus, and Associated Disorders

Clinical Trial Summary

Strabismus (misalignment of the eyes) often runs in families. In this study, the investigators are looking for genetic variants associated with strabismus and nystagmus. Three types of subects will be enrolled: (1) Families with at least 3 members with strabismus, (2) individuals with infantile esotropia and their parents and siblings, and (3) individuals with infantile nystagmus and their parents. Whole exome and/or whole genome sequencing will be used to identify genetic variants shared by family members with strabismus and to identify genetic causes of nystagmus.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04770519
Study type Observational
Source Boston Children's Hospital
Contact Tapiwa Muvavarirwa, BA
Phone 857-292-3768
Email research.whitman@childrens.harvard.edu
Status Recruiting
Phase
Start date September 3, 2021
Completion date December 2026
View Details
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