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Combined Brown syndrome and superior oblique palsy without a trochlear nerve: case report

Cited 4 time in Web of Science Cited 4 time in Scopus
Authors

Yang, Hee Kyung; Kim, Jae Hyoung; Kim, Ji-Soo; Hwang, Jeong-Min

Issue Date
2017-08-25
Publisher
BioMed Central
Citation
BMC Ophthalmology, 17(1):159
Keywords
Brown syndromeSuperior oblique palsyTrochlear nerve
Description
CCDD: congenital cranial dysinnervation disorder; MRI: magnetic resonance imaging; RHT: right hypertropia; SO: superior oblique
Abstract
Abstract

Background
Congenital Brown syndrome is characterized by limited elevation particularly during adduction. The pathogenesis of congenital Brown syndrome is still controversial.

Case presentation
A 6-year-old boy had been tilting his head to the left since infancy. He showed right hypertropia (RHT) of 2 prism diopters (Δ) in the primary position. He showed RHT 6Δ in right gaze, RHT 2Δ in left gaze, RHT 12Δ in right head tilt, and orthotropia in left head tilt. The right eye showed limitation of elevation and depression on adduction, and the left eye showed overdepression on adduction. MR images showed an absent right trochlear nerve with a hypoplastic ipsilateral superior oblique muscle.

Conclusions
Congenital Brown syndrome may be associated with an absent trochlear nerve and hypoplastic superior oblique muscle suggesting an etiologic mechanism of congenital cranial dysinnervation disorder.
ISSN
1471-2415
Language
English
URI
https://hdl.handle.net/10371/138287
DOI
https://doi.org/10.1186/s12886-017-0553-9
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