Defining subphenotypes for oral clefts based on dental development

Journal of Dental Research

Volumn 86, Issue 10, 2007, Pages 986-991

  Letra, A ^a,b,c   Menezes, R ^a   Granjeiro, J M ^d   Vieira, A R ^a  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

^c Bolsista CAPES/BEX   (Brazil)

^d FLUMINENSE FEDERAL UNIVERSITY   (Brazil)

Author keywords

Agenesis; Cleft lip; Cleft palate; Dental anomalies; Oral clefts; Subphenotype

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CASE CONTROL STUDY; CHI SQUARE DISTRIBUTION; CHILD; CLASSIFICATION; CLEFT LIP; CLEFT PALATE; CONGENITAL MALFORMATION; GENETICS; HUMAN; INCISOR; JAW; MIDDLE AGED; NONPARAMETRIC TEST; PHENOTYPE; PRESCHOOL CHILD; RISK; TOOTH MALFORMATION;

ADOLESCENT; ADULT; ALVEOLAR PROCESS; CASE-CONTROL STUDIES; CHI-SQUARE DISTRIBUTION; CHILD; CHILD, PRESCHOOL; CLEFT LIP; CLEFT PALATE; HUMANS; INCISOR; MIDDLE AGED; ODDS RATIO; PHENOTYPE; STATISTICS, NONPARAMETRIC; TOOTH ABNORMALITIES;

EID: 35348870990     PISSN: 00220345     EISSN: None     Source Type: Journal    
DOI: 10.1177/154405910708601013     Document Type: Article

References (26)

1. Adams MS, Niswander JD (1967). Developmental 'noise' and a congenital malformation. Genet Res 10:313-317.
2. Aizenbud D, Camasuvi S, Peled M, Brin I (2005). Congenitally missing teeth in the Israeli cleft population. Cleft Palate Craniofac J 42:314-317.
3. Avila JR, Jezewski PA, Vieira AR, Orioli IM, Castilla EE, Christensen K, et al. (2006). PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations. Am J Med Genet A 140:2562-2570.
4. Eerens K, Vlietinck R, Heidbuchel K, Van Olmen A, Derom C, Willems G, et al. (2001). Hypodontia and tooth formation in groups of children with cleft, siblings without cleft, and nonrelated controls. Cleft Palate Craniofac J 38:374-378.
5. Fogh-Andersen P (1942). Inheritance of harelip and cleft palate. Copenhagen: Arnold Busck.
6. Jordan RE, Kraus BS, Neptune CM (1966). Dental abnormalities associated with cleft lip and/or palate. Cleft Palate J 3:22-25.
7. Larmour CJ, Mossey PA, Thind BS, Forgie AH, Stirrups DR (2005). Hypodontia - a retrospective review of prevalence and etiology. Part I. Quintessence Int 36:263-270.
8. Nieminen P, Arte S, Pirinen S, Peltonen L, Thesleff I (1995). Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes. Hum Genet 96:305-308.
9. Ranta R (1982). Comparison of tooth formation in non-cleft and cleft-affected children with and without hypodontia. ASDC J Dent Child 49:197-199.
10. Ranta R (1983), Hypodontia and delayed development of the second premolars in cleft palate children. Eur J Orthod 5:145-148.
11. Ranta R (1986), A review of tooth formation in children with cleft lip/palate. Am J Orthod Dentofacial Orthop 90:11-18.
12. Rice JP, Saccone NL, Rasmussen E (2001). Definition of the phenotype. In: Genetic dissection of complex traits. Rao DC, Province MA, editors. San Diego: Academic Press, pp. 69-76.
13. Schroeder DC, Green LJ (1975). Frequency of dental trait anomalies in cleft, sibling and non-cleft groups. J Dent Res 54:802-807.
14. Shapira Y, Lubit E, Kuftinec MM (1999). Congenitally missing second premolars in cleft lip and cleft palate children. Am J Orthod Dentofacial Orthop 115:396-400.
15. Shapira Y, Lubit E, Kuftinec MM (2000). Hypodontia in children with various types of clefts. Angle Orthod 70:16-21.
16. Shprintzen RJ, Siegel-Sadewitz VL, Amato J, Goldberg RB (1985). Anomalies associated with cleft lip, cleft palate, or both. Am J Med Genet 20:585-595.
17. Slayton RL, Williams L, Murray JC, Wheeler JJ, Lidral AC, Nishimura CJ (2003). Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region. Cleft Palate Craniofac J 40:274-279.
18. Stahl F, Grabowski R, Wigger K (2006). Epidemiology of Hoffmeister's "genetically determined predisposition to disturbed development of the dentition" in patients with cleft lip and palate. Cleft Palate Craniofac J 43:457-465.
19. Tsai TP, Huang CS, Huang CC, See LC (1998). Distribution patterns of primary and permanent dentition in children with unilateral complete cleft lip and palate. Cleft Palate Craniofac J 35:154-160.
20. van den Boogard MJ, Dorland M, Beemer FA, van Amstel HK (2000). MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat Genet 24:342-343.
21. Vieira AR (2003). Oral clefts and syndromic forms of tooth agenesis as models for genetics of isolated tooth agenesis. J Dent Res 82:162-165.
22. Vieira AR, Orioli IM, Castilla EE, Cooper ME, Marazita ML, Murray JC (2003). MSX1 and TGFB3 contribute to clefting in South America. J Dent Res 82:289-292.
23. Vieira AR, Avila JR, Daack-Hirsch S, Dragan E, Felix TM, Rahimov F, et al. (2005). Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. PLoS Genet 1 :e64.
24. Warrington A, Vieira AR, Christensen K, Orioli IM, Castilla EE, Romitti PA, et al. (2006). Genetic evidence for the role of loci at 19q13 in cleft lip and palate. J Med Genet 43:e26.
25. Weinberg SM, Neiswanger K, Martin R, Mooney MP, Kane AA, Wenger SL, (2006). The Pittsburgh Oral-Facial Cleft Study: expanding the cleft phenotype. Background and justification. Cleft Palate Craniofac J 43:7-20.
26. Werner SP, Harris EF (1989). Odontometrics of the permanent teeth in cleft lip and palate: systemic size reduction and amplified asymmetry. Cleft Palate J 26:36-41.