1. Inner-ear malformations as a cause of single-sided deafness.
- Author
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Tahir, E, Bajin, M D, Jafarov, S, Yıldırım, M Ö, Çınar, B Ç, Sennaroğlu, G, and Sennaroğlu, L
- Subjects
RISK of deafness ,ACOUSTIC nerve ,COCHLEA ,COMPUTED tomography ,DEAFNESS ,EAR canal ,INNER ear ,MAGNETIC resonance imaging ,RETROSPECTIVE studies ,DESCRIPTIVE statistics - Abstract
Objective: To determine the prevalence and distribution of inner-ear malformations in congenital single-sided deafness cases, as details of malformation type are crucial for disease prognosis and management. Methods: A retrospective study was conducted of 90 patients aged under 16 years with congenital single-sided deafness. Radiological findings were evaluated using computed tomography and magnetic resonance imaging. Inner-ear malformations were identified and cochlear nerve status was determined in affected ears. Results: Out of 90 ears, 42 (46.7 per cent) were found to have inner-ear malformation. Isolated cochlear aperture stenosis was the most common anomaly (n = 18, 20 per cent), followed by isolated cochlear aperture atresia (n = 11, 12.2 per cent) and cochlear hypoplasia (n = 7, 7.8 per cent). Cochlear nerve deficiency was encountered in 41 ears (45.6 per cent). The internal auditory canal was also stenotic in 49 ears (54.4 per cent). Conclusion: Inner-ear malformations, especially cochlear aperture anomalies, are involved in the aetiology of single-sided deafness more than expected. The cause of single-sided deafness differs greatly between congenital and adult-onset cases. All children with single-sided deafness should undergo radiological evaluation, as the prognosis and management, as well as the aetiology, may be significantly influenced by inner-ear malformation type. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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