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Published on: March 1, 2015
Congenitally dysplastic inferior rectus muscle
Ramesh Kekunnaya1, Rasheena Bansal, Geeta K Vemuganti
1Jasti V Ramanamma Children’s Eye Care Center, L. V. Prasad Eye Institute, Hyderabad, India. drrk123@gmail.com
Insights
This study details a rare case of congenital inferior rectus muscle dysplasia in a child. Surgical correction successfully treated the associated hypotropia and enophthalmos.
Area of Science:
- Ophthalmology
- Pediatric Ophthalmology
- Strabismus Surgery
Background:
- Isolated unilateral enlargement of extraocular muscles in children is uncommon with no clear etiology.
- Congenital muscular anomalies can present with complex ophthalmic manifestations.
Observation:
- A 20-month-old child presented with a congenitally enlarged posterior inferior rectus muscle, causing hypotropia and enophthalmos since 10 months of age.
- Preoperative assessment revealed severe right eye hypotropia and globe retraction.
- Computed tomography showed inferior rectus muscle thickening; biopsy revealed non-specific fibrotic changes.
Findings:
- Surgical correction of the dysplastic inferior rectus muscle was performed at 2 years of age.
- Postoperatively, the child experienced significant reduction in hypotropia.
- Elimination of the compensatory head position was observed.
Implications:
- This case highlights surgical correction as an effective treatment for congenital inferior rectus muscle dysplasia.
- Early surgical intervention can improve ocular alignment and reduce secondary compensatory mechanisms.
- Further research into the etiology of idiopathic extraocular muscle enlargement is warranted.
Abstract:
The authors report an unusual presentation of an idiopathic congenitally dysplastic inferior rectus muscle that responded well to surgical correction. Isolated unilateral enlargement of extraocular muscles is rare in children, and there is no definite logical explanation for its cause. A 20-month-old child presented with a congenitally enlarged posterior part of the right inferior rectus muscle with prominent hypotropia and enophthalmos since 10 months of age. Systemic disease work-up, ultrasound B-scan, computed tomography of the orbit and brain, and inferior rectus muscle biopsy were performed. Preoperatively, the child had severe hypotropia of the right eye with retraction of the globe. Work-up for systemic diseases was negative. Computed tomography scan showed thickening of the posterior two-thirds of the inferior rectus muscle. Muscle biopsy showed non-specific fibrotic changes. Strabismus surgery was undertaken at 2 years of age. Hypotropia was reduced significantly postoperatively. Compensatory head position was eliminated.
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