Rubinstein-taybi syndrome: A case report
Göster/ Aç
Erişim
info:eu-repo/semantics/openAccessAttribution 3.0 United Stateshttp://creativecommons.org/licenses/by/3.0/us/Tarih
2012Üst veri
Tüm öğe kaydını gösterKünye
Patır Münevveroğlu, A. ve Ballı Akgöl, B. (2012). Rubinstein-taybi syndrome: A case report. Case Reports in Dentistry, 2012. https://dx.doi.org/10.1155/2012/483867Özet
Rubinstein-Taybi syndrome or Broad Thumb-Hallux syndrome is a genetic disorder characterized by facial dysmorphism, growth retardation, and mental deficiency. A seven-year-old girl had come to the Department of Pedodontics, Istanbul Medipol University, Faculty of Dentistry, Turkey, with a complaint of caries and bleeding of gingivae. The patient was mentally retarded. Extraoral features revealed distinctive facial appearance with a broad fore head, hypertelorism, broad nasal bridge, and beaked nose. Intraoral features observed were talons cusps in the upper lateral incisors, carious teeth, and plaque accumulation. Since the patient was mentally retarded, the dental treatment was done under GA. The treatment plan and dental management of this patient are discussed in this case report.
Kaynak
Case Reports in DentistryCilt
2012Koleksiyonlar
- Makale Koleksiyonu [545]
- PubMed İndeksli Yayınlar Koleksiyonu [4039]
- WoS İndeksli Yayınlar Koleksiyonu [6417]
Aşağıdaki lisans dosyası bu öğe ile ilişkilidir: