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    An interdisciplinary approach in a patient with amelogenesis imperfecta: A clinical report and literatüre review
    (2012) Ulku S.Z.B.; Callea M.; Yavuz I.; Clarich G.; Kaya F.A.; Maglione M.; Kaya S.
    This clinical report describes an interdisciplinary approach for the coordinated treatment of a 20-year-old woman patient diagnosed with amelogenesis imperfecta. The treatment objective was to restore masticatory function, to reduce dental sensitivity and improve the facial esthetics. A multidisciplinary team approach treatment is recommended, including periodontology, orthodontics, endodontics, and prosthodontics. Prosthodontic treatment included composite laminate veneers and metal-ceramic fixed partial dentures. After treatment the patient was regularly recalled during the 25-months postoperative period. Radiographic and clinical examinations at recall revealed no evidence of complications associated with the restored teeth or their supporting structures.
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    An unusual case: Neurofibromatosis type 5
    (2012) Callea M.; Ulku S.Z.B.; Giustini S.; Yavuz I.; Ulku M.M.; Montanari M.; Basaran G.
    Neurofibromatosis is a disease which includes 5 types in its classification. It has been firstly described by Robert Smith in 1849, but its name comes from the first publication in 1882, in which Von Recklinghausen convinced the scientific and medical world that Neurofibromatosis (NF) was a distinct entity. Cafe-au-lait spots, cutaneous neurofibromas and Lisch nodules are the characteristics of the most common forms. Bilateral acoustic neuromas distinguish the type 2. Type 3, Riccardi type and intestinal type are briefly described. Neurofibromatosis type 5 (NF5) is characterized by cafe-au-lait spots restricted to one area of the body. We report oro-dental phenotype of a patient affected by NF type 5, rare per se and unreported in literature.