Oro-dental features as useful diagnostic tool in Rubinstein-Taybi syndrome

被引:22
作者
Bloch-Zupan, A.
Stachtou, J.
Emmanouil, D.
Arveiler, B.
Griffiths, D.
Lacombe, D.
机构
[1] Univ Strasbourg, Fac Chirurg Dent Strasbourg, F-67000 Strasbourg, France
[2] CHU Strasbourg, Ctr Reference Manifestat Odontol Malad Rares, F-67000 Strasbourg, France
[3] IGBMC, Dept Genet & Physiol Signalisat Nucl, Illkirch Graffenstaden, France
[4] UCL, Eastman Dent Inst, London, England
[5] UCL, Inst Child Hlth, London, England
[6] Univ Athens, Sch Dent, Dept Paediat Dent, Athens, Greece
[7] Univ Victor Segalen, CHU Bordeaux, Pellegrin Enfants Hosp, Dept Med Genet, Bordeaux, France
关键词
Rubinstein-Taybi syndrome; phenotype; tooth abnormalities; talon cusps;
D O I
10.1002/ajmg.a.31622
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Rubinstein-Taybi syndrome (RTS; OMIM #180849) is a well-known disorder characterized by mental and growth retardation, broad thumbs and great toes, and unusual facial characteristics. We studied oro-dental findings in a group of RTS patients: 12 from the UK, 2 from Greece, and 26 from France. All were examined by two investigators, using the Diagnosing Dental Defects Database record form to document these. Various oro-dental features were found: small mouth, retrognathia, micrognathia, highly arched and narrow palate, talon cusps, expressed crowding, screwdriver incisors, cross bites, and enamel hypoplasia. Eruption was usually normal. Specific attention for these anomalies should facilitate diagnosis and help adequate management. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:570 / 573
页数:4
相关论文
共 15 条
[1]   Unusual case of bilateral talon cusp associated with dens invaginatus [J].
de Sousa, SMG ;
Tavano, SMR ;
Bramante, CM .
INTERNATIONAL ENDODONTIC JOURNAL, 1999, 32 (06) :494-498
[2]  
Hattab F N, 1998, J Clin Pediatr Dent, V22, P159
[3]  
HENNEKAM RCM, 1990, AM J MED GENET, P42
[4]  
Lorena Simone Cristina Martins, 2003, J Oral Sci, V45, P47
[5]  
Mavrodisz Katalin, 2003, Fogorv Sz, V96, P257
[6]   Localization of transcriptional co-activator CBP in the ameloblasts and the other enamel organ-derived cells of the rat incisor [J].
Nishikawa, S .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2002, 50 (11) :1455-1460
[7]   Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism [J].
Oike, Y ;
Hata, A ;
Mamiya, T ;
Kaname, T ;
Noda, Y ;
Suzuki, M ;
Yasue, H ;
Nabeshima, T ;
Araki, K ;
Yamamura, K .
HUMAN MOLECULAR GENETICS, 1999, 8 (03) :387-396
[8]  
Partanen M, 1999, INT J DEV BIOL, V43, P487
[9]  
RUBINSTEIN JH, 1990, AM J MED GENET, P3
[10]   BROAD THUMBS AND TOES AND FACIAL ABNORMALITIES - A POSSIBLE MENTAL RETARDATION SYNDROME [J].
RUBINSTEIN, JH ;
TAYBI, H .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1963, 105 (06) :588-+