Abstract
BackgroundWe have previously reported that the presence of the abducens nerve was variable in patients with type 3 Duane’s retraction syndrome (DRS), being present in 2 of 5 eyes (40%) and absent in 3 (60%) on magnetic resonance imaging (MRI). The previous study included only 5 eyes with unilateral DRS type 3.ObjectivesTo supplement existing scarce pathologic information by evaluating the presence of the abducens nerve using high resolution thin-section MRI system in a larger number of patients with DRS type 3, thus to provide further insight into the pathogenesis of DRS.Data ExtractionA retrospective review of medical records on ophthalmologic examination and high resolution thin-section MRI at the brainstem level and orbit was performed. A total of 31 patients who showed the typical signs of DRS type 3, including abduction and adduction deficit, globe retraction, narrowing of fissure on adduction and upshoot and/or downshoot, were included. The abducens nerve and any other extraocular muscle abnormalities discovered by MRI were noted.ResultsDRS was unilateral in 26 patients (84%) and bilateral in 5 patients (16%). Two out of 5 bilateral patients had DRS type 3 in the right eye and DRS type 1 in the left eye. Of the 34 affected orbits with DRS type 3 in 31 patients, the abducens nerve was absent or hypoplastic in 31 eyes (91%) and present in 3 eyes (9%). Patients with a present abducens nerve showed more limitation in adduction compared to patients with an absent abducens nerve (P = 0.030).ConclusionsThe abducens nerve is absent or hypoplastic in 91% of DRS type 3. Patients with a present abducens nerve showed more prominent limitation of adduction. As DRS type 3 partly share the same pathophysiology with type 1 and 2 DRS, the classification of DRS may have to be revised according to MRI findings.
Highlights
Duane’s retraction syndrome (DRS) consists of a congenital limited abduction and/or adduction, and narrowing of the palpebral fissure, eyeball retraction, and upshoots or downshoots of the affected eye on adduction.[1]
DRS was unilateral in 26 patients (84%) and bilateral in 5 patients (16%)
As DRS type 3 partly share the same pathophysiology with type 1 and 2 DRS, the classification of DRS may have to be revised according to magnetic resonance imaging (MRI) findings
Summary
Duane’s retraction syndrome (DRS) consists of a congenital limited abduction and/or adduction, and narrowing of the palpebral fissure, eyeball retraction, and upshoots or downshoots of the affected eye on adduction.[1]. OPEN ACCESS Citation: Yang HK, Kim JH, Hwang J-M (2016) Abducens Nerve in Patients with Type 3 Duane’s Retraction Syndrome. We have previously reported that the presence of the abducens nerve was variable in patients with type 3 Duane’s retraction syndrome (DRS), being present in 2 of 5 eyes (40%) and absent in 3 (60%) on magnetic resonance imaging (MRI). The previous study included only 5 eyes with unilateral DRS type 3
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