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

DC Field Value Language
dc.contributor.authorYang, Hee Kyung-
dc.contributor.authorKim, Jae Hyoung-
dc.contributor.authorKim, Ji-Soo-
dc.contributor.authorHwang, Jeong-Min-
dc.date.accessioned2017-11-02T02:13:14Z-
dc.date.available2017-11-02T11:14:19Z-
dc.date.issued2017-08-25-
dc.identifier.citationBMC Ophthalmology, 17(1):159ko_KR
dc.identifier.issn1471-2415-
dc.identifier.urihttps://hdl.handle.net/10371/138287-
dc.descriptionCCDD: congenital cranial dysinnervation disorder; MRI: magnetic resonance imaging; RHT: right hypertropia; SO: superior obliqueko_KR
dc.description.abstractAbstract

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.
ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Centralko_KR
dc.subjectBrown syndromeko_KR
dc.subjectSuperior oblique palsyko_KR
dc.subjectTrochlear nerveko_KR
dc.titleCombined Brown syndrome and superior oblique palsy without a trochlear nerve: case reportko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor양희경-
dc.contributor.AlternativeAuthor김재형-
dc.contributor.AlternativeAuthor김지수-
dc.contributor.AlternativeAuthor황정민-
dc.identifier.doi10.1186/s12886-017-0553-9-
dc.language.rfc3066en-
dc.rights.holderThe Author(s).-
dc.date.updated2017-10-03T16:49:41Z-
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