Evidence map›Paper›PMID 41735562›Full record

ArticleEuropean archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery2026

Anomalous posterior semicircular canals in congenital hearing loss: not-so-common findings in a common imaging scenario!

Harsimran Bhatia, Purnima Agarwal, Shashikant Pol

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Article in European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Harsimran BhatiaDepartment of Radiodiagnosis and Imaging, Post Graduate Institute of Medical Education and Research, Chandigarh, 160012, India. harsimranbhatia13@gmail.com.ORCID http://orcid.org/0000-0002-0228-9771
Purnima AgarwalDepartment of Radiodiagnosis and Imaging, Government Medical College and Hospital, Sector 32, Chandigarh, India.
Shashikant PolDepartment of ENT and head neck surgery, Velammal Medical College Hospital and Research Institute, Madurai, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital SNHL cases often undergo imaging to rule out malformations of the inner ear. Semicircular (SCC) anomalies constitute one such important group with posterior SCC being rarely affected. We describe a radiological spectrum of anomalous posterior SCCs in three cases with congenital SNHL. CASE

findingsAll three cases were children < 14 years of age and underwent HRCT and MRI with a variable degree of anomalies affecting the posterior SCC. The first case had aplasia of left post SCC with findings of Type I Incomplete partition. Second case showed isolated posterior SCC hypoplasia bilaterally with no other inner ear malformation on imaging. Third case revealed findings of a dysplastic left posterior SCC with features of Type I Incomplete partition. DISCUSSION: These three cases represent a unique imaging spectrum resulting from an arrest at various stages of embryological development of post SCC. These anomalies often accompanyother inner ear malformations (IEMs) and systemic syndromes.

conclusionComprehensive imaging with CT and MRI is essential to determine the presence and degree of IEMs as well as to ascertain the status of cochlear nerve in determining feasibility for cochlear implantation.

Indexed as

Hearing Loss, SensorineuralSemicircular CanalsAdolescentChildChild, PreschoolFemaleHumansMagnetic Resonance ImagingMaleTomography, X-Ray ComputedCongenitalImagingInner earPosterior semicircular canal

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.