Pyriform aperture enlargement in all aspects

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dc.contributor.authorEsen, E.
dc.contributor.authorMuluk, N. Bayar
dc.contributor.authorAltintoprak, N.
dc.contributor.authorIpci, K.
dc.contributor.authorCingi, C.
dc.date.accessioned2020-06-25T18:22:59Z
dc.date.available2020-06-25T18:22:59Z
dc.date.issued2017
dc.departmentKırıkkale Üniversitesi
dc.description.abstractBackground: The pyriform aperture comprises the central area of facial bone structure. It is formed by the free corners of the nasal bone and the frontal processes of the maxillae, which articulate with each other at the nasomaxillary suture lines. Congenital nasal pyriform aperture stenosis might be linked to various craniofacial problems. This review presents all aspects of pyriform aperture stenosis and enlargement. Methods: A literature search was conducted. Pyriform aperture definition, nasal development, congenital nasal pyriform aperture stenosis and pyriform aperture enlargement were reviewed. Results: One of the most common abnormalities is holoprosencephaly, which is a midline developmental deficiency that may also be present in combination with facial clefting. The aetiology of nasal pyriform aperture stenosis remains unclear. When diagnosed, the choice of treatment is between non-surgical and operative methods, depending on the seriousness of the problem. Provided the sufferer can maintain a secure air passage with the help of specialised medical procedures and respiratory tract adjuvants, operative therapy may be delayed. Conclusion: The operative outcomes are extremely good, and the prognosis relies mainly on coexisting neural and endocrine problems. This paper evaluates the nasal pyriform aperture in detail.en_US
dc.description.sponsorshipContinuous Education and Scientific Research Associationen_US
dc.description.sponsorshipThe preparation of this paper, including its design and planning, was supported by the Continuous Education and Scientific Research Association.en_US
dc.identifier.citationclosedAccessen_US
dc.identifier.doi10.1017/S0022215117000391
dc.identifier.endpage479en_US
dc.identifier.issn0022-2151
dc.identifier.issn1748-5460
dc.identifier.issue6en_US
dc.identifier.pmid28238296
dc.identifier.scopus2-s2.0-85013913536
dc.identifier.scopusqualityQ2
dc.identifier.startpage476en_US
dc.identifier.urihttps://doi.org/10.1017/S0022215117000391
dc.identifier.urihttps://hdl.handle.net/20.500.12587/6973
dc.identifier.volume131en_US
dc.identifier.wosWOS:000435339400004
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherCambridge Univ Pressen_US
dc.relation.ispartofJournal Of Laryngology And Otology
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCongenital Abnormalitiesen_US
dc.subjectFacial Bonesen_US
dc.subjectMaxillaen_US
dc.subjectNoseen_US
dc.subjectStenosisen_US
dc.titlePyriform aperture enlargement in all aspectsen_US
dc.typeReview Article

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