Osteopetrosis complicated by osteomyelitis of the maxilla: A rare case report and review of the literature

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dc.contributor.authorSallies, Moegamat
dc.contributor.authorTitinchi, Fadi
dc.contributor.authorMorkel, Jean A
dc.date.accessioned2020-11-10T11:21:24Z
dc.date.available2020-11-10T11:21:24Z
dc.date.issued2020
dc.description.abstractOsteopetrosis is a rare hereditary bone disorder that results in an increase in bone density due to gene mutations and osteoclastic dysfunction. This may lead to cranial nerve compression, bone fractures and osteomyelitis. Osteomyelitis of the maxilla is rare even in osteopetrosis patients.en_US
dc.identifier.citationSallies, M. et al. (2020). Osteopetrosis complicated by osteomyelitis of the maxilla: A rare case report and review of the literature. Dental and Medical Problems, 57(3),327-332. Doi: 10.17219/dmp/119998en_US
dc.identifier.issn2300-9020
dc.identifier.urihttp://hdl.handle.net/10566/5407
dc.language.isoenen_US
dc.publisherWroclaw Medical Universityen_US
dc.subjectMaxillaen_US
dc.subjectOsteomyelitisen_US
dc.subjectOsteopetrosisen_US
dc.titleOsteopetrosis complicated by osteomyelitis of the maxilla: A rare case report and review of the literatureen_US
dc.title.alternativeOsteopetroza powikłana zapaleniem szpiku szczęki – opis rzadkiego przypadku i przegląd piśmiennictwaen_US
dc.typeArticleen_US

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