Congenitally dysplastic inferior rectus muscle.

dc.contributor.author Kekunnaya, Ramesh
dc.contributor.author Bansal, Rasheena
dc.contributor.author Vemuganti, Geeta K.
dc.date.accessioned 2022-03-27T04:12:09Z
dc.date.available 2022-03-27T04:12:09Z
dc.date.issued 2010-01-01
dc.description.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. Copyright 2010, SLACK Incorporated.
dc.identifier.citation Journal of pediatric ophthalmology and strabismus. v.47 Online
dc.identifier.uri 10.3928/01913913-20100719-10
dc.identifier.uri http://www.slackinc.com/doi/resolver.asp?doi=10.3928/01913913-20100719-10
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/6859
dc.title Congenitally dysplastic inferior rectus muscle.
dc.type Journal. Article
dspace.entity.type
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