Djerić, Dragoslava (7006706299)Dragoslava (7006706299)DjerićCvorović, Ljiljana (16229375800)Ljiljana (16229375800)CvorovićBlažić, Srbislav (55156429000)Srbislav (55156429000)Blažić2025-06-122025-06-122015https://doi.org/10.2298/SARH1502068Dhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84924351622&doi=10.2298%2fSARH1502068D&partnerID=40&md5=e3ac9d1eb5390efabd3589982bc7e5e6https://remedy.med.bg.ac.rs/handle/123456789/8538Introduction 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.Bilateral congenital cholesteatomaCrouzon syndromeHearing loss