Rubinstein-taybi syndrome: A case report
View/ Open
Access
info:eu-repo/semantics/openAccessAttribution 3.0 United Stateshttp://creativecommons.org/licenses/by/3.0/us/Date
2012Metadata
Show full item recordCitation
Patır Münevveroğlu, A. ve Ballı Akgöl, B. (2012). Rubinstein-taybi syndrome: A case report. Case Reports in Dentistry, 2012. https://dx.doi.org/10.1155/2012/483867Abstract
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.
Source
Case Reports in DentistryVolume
2012Collections
- Makale Koleksiyonu [546]
- PubMed İndeksli Yayınlar Koleksiyonu [4047]
- WoS İndeksli Yayınlar Koleksiyonu [6432]
The following license files are associated with this item: