Sphenoid sinus agenesis and sella turcica hypoplasia: very rare cases of two brothers with Hamamy syndrome

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dc.authoridduman, suayip burak/0000-0003-2552-0187
dc.authoridaltun, oguzhan/0000-0002-5020-8032
dc.authoriddedeoğlu, numan/0000-0003-0892-3654
dc.authorwosidduman, suayip burak/ABE-5878-2020
dc.authorwosidArıkan, Büşra/ABH-4769-2020
dc.authorwosidaltun, oguzhan/ABH-4382-2020
dc.authorwosiddedeoğlu, numan/ABH-2864-2020
dc.contributor.authorDuman, Suayip Burak
dc.contributor.authorDedeoglu, Numan
dc.contributor.authorArikan, Busra
dc.contributor.authorAltun, Oguzhan
dc.date.accessioned2024-08-04T20:48:53Z
dc.date.available2024-08-04T20:48:53Z
dc.date.issued2020
dc.departmentİnönü Üniversitesien_US
dc.description.abstractHamamy syndrome (HS) is an autosomal recessive syndrome with a genetic origin that is very rarely observed. The syndrome with craniofacial dysmorphisms, including midface prominence, severe telecanthus, sparse lateral eyebrows, protruding ears, fronto-nasal abnormalities, lacrimal-salivary apparatus agenesis, thin upper vermillion border, myopia, mental retardation, sensorineural hearing impairment, congenital heart anomalies with intraventricular conduction delay, hypochromic microcytic anaemia and skeletal abnormalities of the long bones with recurrent fractures. In this paper, we report a case of two brothers diagnosed with HS at the ages of 25 and 18 years, visited out clinic at different times due to dental reasons. In the radiological examinations, it was observed that both brothers have sphenoid sinuses agenesia, and their sella turcica were smaller than normal. HS may be observed very rarely, and it should be kept in mind that, in addition to various symptoms, it may also cause sphenoid sinus agenesis and sella turcica hypoplasia as shown for the first time in this case report.en_US
dc.identifier.doi10.1007/s00276-020-02558-9
dc.identifier.endpage1380en_US
dc.identifier.issn0930-1038
dc.identifier.issn1279-8517
dc.identifier.issue11en_US
dc.identifier.pmid32860086en_US
dc.identifier.scopus2-s2.0-85089973579en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage1377en_US
dc.identifier.urihttps://doi.org/10.1007/s00276-020-02558-9
dc.identifier.urihttps://hdl.handle.net/11616/99502
dc.identifier.volume42en_US
dc.identifier.wosWOS:000563807100001en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherSpringer Franceen_US
dc.relation.ispartofSurgical and Radiologic Anatomyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHamamy syndromeen_US
dc.subjectSella turcicaen_US
dc.subjectSphenoid sinus agenesisen_US
dc.titleSphenoid sinus agenesis and sella turcica hypoplasia: very rare cases of two brothers with Hamamy syndromeen_US
dc.typeArticleen_US

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