{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,26]],"date-time":"2025-12-26T03:57:00Z","timestamp":1766721420808,"version":"3.48.0"},"reference-count":19,"publisher":"MDPI AG","issue":"1","license":[{"start":{"date-parts":[[2025,12,23]],"date-time":"2025-12-23T00:00:00Z","timestamp":1766448000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Audiology Research"],"abstract":"<jats:p>Background and Clinical Significance: Vestibular disorders in children are often overlooked, delaying treatment. Early diagnosis of benign paroxysmal positional vertigo (BPPV) allows for targeted maneuvers during acute episodes. Though rare, BPPV can occur in children due to stereocilin gene (STRC) deletions or variants, causing hearing loss and vestibular dysfunction. Case Presentation: This study highlights a case of recurrent vertigo linked to a homozygous deletion on chromosome 15 affecting the STRC gene.<\/jats:p>","DOI":"10.3390\/audiolres16010004","type":"journal-article","created":{"date-parts":[[2025,12,23]],"date-time":"2025-12-23T14:05:22Z","timestamp":1766498722000},"page":"4","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Positional Vertigo in a Child with Hearing Loss"],"prefix":"10.3390","volume":"16","author":[{"ORCID":"https:\/\/orcid.org\/0009-0008-9982-7951","authenticated-orcid":false,"given":"Melissa","family":"Blanco-Pareja","sequence":"first","affiliation":[{"name":"Department of Otorhinolaryngology, Cl\u00ednica Universidad de Navarra, 28022 Madrid, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0258-1761","authenticated-orcid":false,"given":"Alberto","family":"Vieco Garc\u00eda","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Cl\u00ednica Universidad de Navarra, 28022 Madrid, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5825-0166","authenticated-orcid":false,"given":"Teresa","family":"Perucho","sequence":"additional","affiliation":[{"name":"Deaprtment of Genetics, Cl\u00ednica Universidad de Navarra, 28022 Madrid, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0002-4275-2545","authenticated-orcid":false,"given":"Javier","family":"Santos","sequence":"additional","affiliation":[{"name":"Department of Otorhinolaryngology, Cl\u00ednica Universidad de Navarra, 28022 Madrid, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1513-6579","authenticated-orcid":false,"given":"Jos\u00e9 Manuel","family":"Moreno-Villares","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Cl\u00ednica Universidad de Navarra, 28022 Madrid, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1192-5901","authenticated-orcid":false,"given":"Nicolas","family":"P\u00e9rez-Fern\u00e1ndez","sequence":"additional","affiliation":[{"name":"Department of Otorhinolaryngology, Cl\u00ednica Universidad de Navarra, 28022 Madrid, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1968","published-online":{"date-parts":[[2025,12,23]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"1871","DOI":"10.1038\/s41431-018-0256-6","article-title":"Stereocilin gene variants associated with episodic vertigo: Expansion of the DFNB16 phenotype","volume":"26","author":"Frykholm","year":"2018","journal-title":"Eur. 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