Current Views on the Development of the Tympanal Segment of the Facial Nerve

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dc.creatorBakhramdjanovich, Gulyamov Sherzod
dc.date2024-05-31
dc.date.accessioned2024-10-12T12:36:15Z
dc.date.available2024-10-12T12:36:15Z
dc.descriptionEar canal atresia is a congenital or acquired obliteration of the bony cartilaginous canal that connects the auricle to the middle ear. Closure of the auditory canal is accompanied by a decrease in hearing acuity up to deafness. Congenital atresia is often combined with microtia and other developmental anomalies. Diagnosis includes examination by an otolaryngologist with otoscopy, audiometry and computed tomography of the temporal bone. In case of bony overgrowths, skull radiography is performed. Treatment of pathology is surgical. During surgery, an artificial canal is formed using skin and cartilage flaps; if necessary, tympanoplasty is performed. Anomalies of the auricle require plastic reconstructive surgery.en-US
dc.formatapplication/pdf
dc.identifierhttps://journals.proindex.uz/index.php/JSML/article/view/1126
dc.identifier.urihttps://dspace.umsida.ac.id/handle/123456789/37601
dc.languageeng
dc.publisherPro Indexen-US
dc.relationhttps://journals.proindex.uz/index.php/JSML/article/view/1126/958
dc.sourceJournal of Science in Medicine and Life; Vol. 2 No. 5 (2024): Journal of Science in Medicine and Life; 517-520en-US
dc.source2992-9202
dc.subjectcongenitalen-US
dc.subjectanomalyen-US
dc.subjectatresia of the external auditory canalen-US
dc.subjectfacial nerveen-US
dc.subjectaberrationen-US
dc.titleCurrent Views on the Development of the Tympanal Segment of the Facial Nerveen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Articleen-US
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