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Rubinstein-Taybi Syndrome: A Case Report
Author(s) -
Aslı Patır Münevveroğlu,
Beyza Ballı Akgöl
Publication year - 2012
Publication title -
case reports in dentistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.221
H-Index - 11
eISSN - 2090-6447
pISSN - 2090-6455
DOI - 10.1155/2012/483867
Subject(s) - rubinstein–taybi syndrome , medicine , hypertelorism , girl , dentistry , facial dysmorphism , mentally retarded , dental treatments , nose , orthodontics , dermatology , surgery , anatomy , psychology , developmental psychology , biochemistry , chemistry , gene , phenotype
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.

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