Craniofacial features associated with amelogenesis imperfecta

Journal of Craniofacial Genetics and Developmental Biology

Volumn 19, Issue 3, 1999, Pages 148-156

  Cartwright, Alison R ^a   Kula, Katherine ^b   Wright, Tim J ^a,c  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b UNIVERSITY OF MISSOURI KANSAS CITY   (United States)

^c UNIVERSITY OF NORTH CAROLINA   (United States)

Author keywords

Amelogenesis imperfecta; Cephalometric; Craniofacial; Dysmorphology

Indexed keywords

ADOLESCENT; ADULT; AGED; AMELOGENESIS IMPERFECTA; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CEPHALOMETRY; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CRANIOFACIAL MORPHOLOGY; FEMALE; HUMAN; INHERITANCE; MALE; MALOCCLUSION; PHENOTYPE; PRIORITY JOURNAL; SKULL RADIOGRAPHY; UNITED STATES;

EID: 0032747875     PISSN: 02704145     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (34)

1. ALDRED MJ, CRAWFORD PJM: Amelogenesis imperfecta-towards a new classification. Oral Dis 1:2-5, 1995.
2. ALDRED MJ, CRAWFORD PJM, ROBERTS E, GILLESPIE C, THOMAS NST, FENTON I, SANDUIJL LA, HARPER PS: Genetic heterogeneity in X-linked amelogenesis imperfecta Genomics 14:567-573, 1992a.
3. ALDRED MJ, CRAWFORD PJM, ROBERTS E, THOMAS NST: Identification of a nonsense mutation the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1). Hum Genet 90:413-416, 1992b.
4. BACKMAN B, ADOLESSON U: Craniofacial structure related to inheritance pattern in amelogenesis imperfecta Am J Othod Dentofac Orthop 105:575-582, 1994.
5. BEHRENTS RG: An Atlas of Growth in the Aging Craniofacial Skeleton. In "Craniofacial Growth Series", Vol. 18. Ann Arbor, MI: Monogr, 160 p., 1985.
6. BROADBENT BH, GOLDEN WH: "Bolton Standards of Dento-facial Developmental Growth". St Louis: Mosby, 78 p., 1975.
7. CANGIALOSI TJ: Skeletal morphologic features of anterior open bite. Am J Orthod 85:28-36, 1984.
8. COLLIER PM, SAUK JJ, ROSENBLOOM J, YUAN ZA, GIBSON CW: An amelogenin gene defect associated with human x-linked amelogenesis imperfecta. Arch Oral Biol 42:235-242, 1997.
9. COLLINS MA, MAURIELLO SM, TYNDALL DA, WRIGHT JT: Dental anomalies in amelogenesis imperfecta: a radiographic assessment. Oral Surg Oral Med Oral Pathol 1999 (In Press).
10. DUNG DJ, SMITH RJ: Cephalometric and clinical diagnosis of open bite tendency. Am J Orthod Dentofac Orthop 94:484-490, 1988.
11. HARRIS EF, JOHNSON MG: Heritability of craniometric and occlusal variables: a longitudinal sib analysis. Am J Orthod Dentofac Orthop 99:258-268, 1991.
12. HART S, HART T, GIBSON C, WRIGHT JT: Mutational analysis of X-linked amelogenesis imperfecta in multiple families. Arch Oral Biol 1999 (In Press).
13. HOLROYD I, LENCH N, WINTER GB: Amelogenesis imperfecta in triplets: a unique family record. Br Dent J 178:465-468, 1995.
14. HOPPENREIJS TJM, VOORSMIT RACA, FREIHOFER HPM: Open bite deformity in amelogenesis imperfecta Part 1: an analysis of contributory factors and implications for treatment. J Cranio-Maxillo Surg 26:260-266, 1998.
15. KING L, HARRIS EF, TOLLEY EA: Heritability of cephalometric and occlusal variables as assessed from siblings with overt malocclusions. Am J Orthod Dentofac Orthop 104:121-131, 1993.
16. KULA K, HALL KI, HART TC, WRIGHT JT: Craniofacial morphology of the tricho-dento-osseous syndrome. Clin Genet 50:446-454, 1996.
17. LAGERSTROM M, DAHL N, NAKAHORI Y, NAKAGOME Y, BACKMAN B, LANDEGREN U, PETTERSSON U: A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1) Genomics 10:971-975, 1991.
18. LUNDSRTOM A, MCWILLIAM JS: A comparison of vertical and horizontal cephalometric variables with regard to heritability. Eur J Orthod 9:104-108, 1987.
19. MCLAIN JB, PROFFIT WR: Oral health status in the United States: prevalence of malocclusions. J Dent Ed 49:446-496, 1985.
20. OOYA K, NALBANDIAN J, NOIKURA T: Autosomal recessive rough hypoplastic amelogenesis imperfecta: a case report with clinical, light microscopic, radiographic and electron microscopic observations. Oral Surg Oral Med Oral Pathol 65:449-458, 1988.
21. PERSSON M, SUNDELL S: Facial morphology and open bite deformity in amelogenesis imperfecta. Acta Odontol Scand 40:135-144, 1982.
22. PRICE JA, BOWDEN D, WRIGHT JT, PETTENATI MJ, HART T: Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome. Hum Mol Genet 7:563-569, 1998.
23. PROFFIT WR: "Contemporary Orthodontics". St Louis: Mosby, 1986.
24. ROBINSON C, KIRKHAM J, BRIGGS HD, ATKINSON PJ: Enamel proteins from secretion to maturation. J Dent Res 61:1490-1495, 1982.
25. ROWLEY R, HILL FJ, WINTER GB: An investigation of the association between anterior open-bite and amelogenesis imperfecta. Am J Orthod 81:229-235, 1982.
26. SCHULZE A: Developmental abnormalities of teeth and jaws. In Gorlin RJ, Goldman HM (eds): "Thomas Oral Pathology". St Louis: Mosby, 1970.
27. WILLIAMS SA, OGDEN AR: Failure of eruption associated with anomalies of the dentition in siblings. Pediatr Dent 10:130-135, 1988.
28. WINTER GB, BROOK AH: Enamel hypoplasia and anomalies of the enamel. Dent Clin N Amer 19:3-24, 1975.
29. WITKOP CJ: Hereditary defects in enamel and dentin. Acta Genet 7:236-239, 1957.
30. WITKOP CJ, SAUK JJ: Heritable Defects of Enamel. In Stewart R, Prescott G (eds): "Oral Facial Genetics". St Louis: Mosby, pp. 151-226, 1976.
31. WITKOP CJJ: Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited, problems in classification. J Oral Pathol 17:547-553, 1989.
32. WRIGHT JT: Analysis of a kindred with amelogenesis imperfecta. J Oral Pathol 14:366-376, 1985.
33. WRIGHT JT, DEATON TC, HALL KI, YAMAUCHI M: The mineral and protein content of enamel in amelogenesis imperfecta Conn Tissue Res 32:247-252, 1995.
34. WRIGHT JT, KULA K, HALL KI, SIMMONS JH, HART TC: Analysis of the tricho-dento-osseous syndrome genotype and phenotype. Am J Med Genet 72:197-204, 1997.