A common, congenital cranial dysinnervation disorder characterized by limited abduction and adduction to a lesser degree than the other Duane syndrome types. The eye’s ability to move inward toward the nose (adduction) and outward toward the ear (abduction) is limited. Patients present with either exotropia or esotropia in primary gaze.
 

Also Known As

  • Type A Duane's Retraction Syndrome