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dc.contributor.authorTabar, G
dc.contributor.authorKurklu, E
dc.contributor.authorSermet, B
dc.contributor.authorTanyeri, H
dc.contributor.authorDeger, S
dc.date.accessioned2021-03-03T14:57:02Z
dc.date.available2021-03-03T14:57:02Z
dc.date.issued2006
dc.identifier.citationDeger S., Tabar G., Sermet B., Tanyeri H., Kurklu E., "Dental findings and rehabilitation in familial osteodysplasia (Anderson type): a case report", ORAL DISEASES, cilt.12, sa.2, ss.208-212, 2006
dc.identifier.issn1354-523X
dc.identifier.otherav_3c55b564-f30e-40ed-80df-658164ad6ffa
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/44491
dc.identifier.urihttps://doi.org/10.1111/j.1601-0825.2005.01178.x
dc.description.abstractFamilial osteodysplasia is a disorder of osteogenesis with an autosomal recessive pattern of inheritance which predominantly affects facial bones. No recent case had been reported, particularly from a dental point of view since the syndrome was first described by Anderson et al (JAMA 1972;220:1687-93). A 23-year-old male with familial osteodysplasia was presented in maxillofacial and dental aspects with clinical and radiological manifestations including malocclusion, abnormal teeth alignment, impacted teeth, shape disturbances including uncompleted coronal formation, root shortening with bulbous form, high angled mandible and elongation of the corpus of mandible. Recognation of the syndromal features prior to any dental intervention is of paramount importance because of increased inclination to spontaneous mandibular fractures. Hence, no surgical intervention was performed for impacted teeth. Following the extractions of severely mobile teeth, a definitive restoration was fabricated as distal-extension removable partial dentures with conus crown telescopic system. The aesthetic and functional outcome was satisfactory for the patient. In conclusion, dentists appear to play an important role in the recognition of familial osteodysplasia, based on maxillofacial and dentoalveolar findings. Awareness of the syndromal features, especially of spontaneous fractures, would detect the limitations for dental interventions and treatment planning.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectDİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectDiş Hekimliği
dc.titleDental findings and rehabilitation in familial osteodysplasia (Anderson type): a case report
dc.typeMakale
dc.relation.journalORAL DISEASES
dc.contributor.department, ,
dc.identifier.volume12
dc.identifier.issue2
dc.identifier.startpage208
dc.identifier.endpage212
dc.contributor.firstauthorID177976


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