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Congenital absence of the inferior rectus muscle--diagnosis and management.
- Source :
-
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus [J AAPOS] 2003 Oct; Vol. 7 (5), pp. 339-44. - Publication Year :
- 2003
-
Abstract
- Background: Congenital absence of the inferior rectus muscle is a rare cause of apparent inferior rectus palsy especially in the absence of associated cranial facial anomalies.<br />Methods: We report three cases of isolated congenital absence of the inferior rectus muscle and its successful surgical management.<br />Results: Failure of the normal embryologic development of the mesodermal complex around the eye can lead to agenesis of the extraocular muscles. In apparent palsies of the inferior rectus muscle and no definite cause, a high index of suspicion and orbital imaging can confirm the diagnosis of congenitally absent inferior rectus preoperatively. Surgical correction may involve inferior transposition of the horizontal rectus muscles.<br />Conclusions: Although rare, congenital absence of the inferior rectus muscle is a possible cause of apparent inferior rectus muscle palsy particularly in the absence of another identifiable cause. Strabismus surgery in conjunction with intramuscular botulinum toxin injection can offer significant improvement in function and cosmesis of these patients.
- Subjects :
- Adult
Botulinum Toxins, Type A administration & dosage
Congenital Abnormalities diagnosis
Congenital Abnormalities surgery
Female
Humans
Injections, Intramuscular
Male
Neuromuscular Agents administration & dosage
Postoperative Care
Tomography, X-Ray Computed
Treatment Outcome
Oculomotor Muscles abnormalities
Oculomotor Muscles surgery
Subjects
Details
- Language :
- English
- ISSN :
- 1091-8531
- Volume :
- 7
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
- Publication Type :
- Academic Journal
- Accession number :
- 14566316
- Full Text :
- https://doi.org/10.1016/s1091-8531(03)00214-3