{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,16]],"date-time":"2026-02-16T12:08:40Z","timestamp":1771243720288,"version":"3.50.1"},"reference-count":35,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2024,7,29]],"date-time":"2024-07-29T00:00:00Z","timestamp":1722211200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2024,7,29]],"date-time":"2024-07-29T00:00:00Z","timestamp":1722211200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pediatric Pulmonology"],"published-print":{"date-parts":[[2024,12]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>To evaluate otorhinolaryngologic findings and the relationship between aminoglycoside (AG) exposure and hearing loss in paediatric patients with cystic fibrosis (cwCF). We also aimed to investigate the genetic predisposition to AG ototoxicity by screening for m.1555A&gt;G mutations.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>CwCF who underwent otorhinolaryngologic and audiologic examinations were retrospectively included. Clinical characteristics, ear\u2010nose\u2010throat related symptoms, and a history of ototoxic drug exposure were recorded. m.1555A&gt;G mutations were retrospectively screened among patients with audiologic evaluations.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Two hundred thirty\u2010four cwCF were included in this study with a median age of 10.7 (range, 6.8\u201314.2) years. Nasal obstruction (14.1%) was the most common symptom. Fifty\u2010two (22.2%) patients had chronic rhinosinusitis (CRS) with nasal polyps (CRSwNP). There was a positive correlation between CRSwNP and the symptom of nasal obstruction (\n                      <jats:italic>r<\/jats:italic>\n                      :.234,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009&lt;\u2009.001), snoring (\n                      <jats:italic>r<\/jats:italic>\n                      :.179,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u2009.006), and sleeping with mouth open (\n                      <jats:italic>r<\/jats:italic>\n                      :.138,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u2009.034). One hundred forty\u2010nine (63.6%) patients had audiologic evaluations; 14 (9.4%) had hearing impairment. No statistical significance existed between ototoxicity and IV AG exposure (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u2009.90). Six (42.8%) of 14 patients did not receive ototoxic drugs. One hundred nineteen (50.8%) patients were screened for m.1555A&gt;G mutations, and none were detected.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Almost a quarter of the study population had CRSwNP. Neither the relationship between AGs exposure and hearing loss nor the genetic predisposition to AG ototoxicity could be shown in cwCF.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/ppul.27193","type":"journal-article","created":{"date-parts":[[2024,7,29]],"date-time":"2024-07-29T11:20:25Z","timestamp":1722252025000},"page":"3298-3305","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Evaluation of otorhinolaryngologic, audiologic, and genetic findings in children with cystic fibrosis: A tertiary care experience"],"prefix":"10.1002","volume":"59","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6909-7993","authenticated-orcid":false,"given":"Halime","family":"Nay\u0131r B\u00fcy\u00fck\u015fahin","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Division of Pulmonology Hacettepe University Faculty of Medicine Ankara 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