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Bilateral congenital cholesteatoma of the temporal bone in crouzon syndrome

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dc.contributor.authorDjerić, Dragoslava (7006706299)
dc.contributor.authorCvorović, Ljiljana (16229375800)
dc.contributor.authorBlažić, Srbislav (55156429000)
dc.date.accessioned2025-06-12T20:06:59Z
dc.date.available2025-06-12T20:06:59Z
dc.date.issued2015
dc.description.abstractIntroduction Crouzon syndrome is an autosomal dominant genetic disease characterized by bicoronal craniosynostosis, exorbitism with hypertelorism, and maxillary hypoplasia with mandibular prognathism. Case Outline We present the first reported case of Crouzon syndrome associated with a bilateral congenital cholesteatoma of the temporal bone and discuss about the potential pathogenesis. Conclusion Early diagnosis and management are crucial to prevent complications and an otologist should be an integral part of the multidisciplinary team. © 2015 Serbia Medical Society. All rightsreserved.
dc.identifier.urihttps://doi.org/10.2298/SARH1502068D
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84924351622&doi=10.2298%2fSARH1502068D&partnerID=40&md5=e3ac9d1eb5390efabd3589982bc7e5e6
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/8538
dc.subjectBilateral congenital cholesteatoma
dc.subjectCrouzon syndrome
dc.subjectHearing loss
dc.titleBilateral congenital cholesteatoma of the temporal bone in crouzon syndrome
dspace.entity.typePublication

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