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Duane syndrome: An overview on the current management
Priyanka Prasad1, Abhyuday Saxena2, Rohit Saxena1
1Dr. Rajendra Prasad Centre for Ophthalmic Sciences, AIIMS, New Delhi, India.
Duane syndrome, a common congenital strabismus, involves horizontal eye movement deficits and globe retraction. Surgical management must be individualized for optimal outcomes in this congenital cranial dysinnervation disorder.
Area of Science:
- Ophthalmology
- Neurology
- Genetics
Background:
- Duane syndrome is a frequent restrictive congenital strabismus.
- It is characterized by horizontal duction deficits, globe retraction, and eyelid narrowing.
- This condition is now classified as a congenital cranial dysinnervation disorder.
Purpose of the Study:
- To outline the etiopathogenesis and diagnostic criteria for Duane syndrome.
- To discuss the challenges and individualized approaches in surgical management.
- To detail surgical techniques for improving primary gaze alignment and reducing abnormal movements.
Main Methods:
- Diagnosis is primarily clinical, based on characteristic eye movement abnormalities.
- Etiopathogenesis involves dysinnervation of the lateral rectus muscle due to abducens nucleus issues.
- Surgical strategies include differential muscle recessions and Y-split or periosteal fixation.
Main Results:
- Surgical goals include achieving primary gaze alignment, reducing globe retraction, and correcting abnormal head posture.
- Differential recessions of lateral rectus and medial rectus muscles address primary gaze deviations.
- Y-split or periosteal fixation of the lateral rectus muscle manages globe retraction and shoots.
Conclusions:
- Duane syndrome requires individualized surgical planning due to its variable presentation.
- Effective management aims to restore binocularity and improve cosmetic appearance.
- Understanding the underlying dysinnervation guides surgical decision-making for optimal functional and aesthetic results.
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