Inherited enamel defects

CIBA Foundation Symposia

Volumn , Issue 205, 1997, Pages 175-186

  Backman B ^a  

^a UMEÅ UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

AMELOGENESIS IMPERFECTA; CHROMOSOME 4; CHROMOSOME MAP; CLASSIFICATION; EPIDEMIOLOGY; FEMALE; GENETIC LINKAGE; GENETICS; HUMAN; MALE; PATHOLOGY; REVIEW; SWEDEN; X CHROMOSOME;

AMELOGENESIS IMPERFECTA; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 4; EPIDEMIOLOGY, MOLECULAR; FEMALE; HUMANS; LINKAGE (GENETICS); MALE; SWEDEN; X CHROMOSOME;

EID: 0030633110     PISSN: 03005208     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (33)

1. Aldred MJ, Crawford PJM 1995 Amelogenesis imperfecta: towards a new classification. Oral Dis 1:2-5
2. Aldred MJ, Crawford PJM, Roberts E, Thomas NST 1992a Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1). Hum Genet 90:413-416
3. Aldred MJ, Crawford PJM, Roberts E et al 1992b Genetic heterogeneity in X-linked amelogenesis imperfecta. Genomics 14:567-573
4. Bäckman B 1988 Amelogenesis imperfecta: clinical manifestations in 51 families in a northern Swedish county. Scand J Dent Res 96:505-516
5. Bäckman B, Adolfsson U 1994 Craniofacial structure related to inheritance pattern in amelogenesis imperfecta. Am J Orthod Dentofac Orthop 105:575-582
6. Bäckman B, Angmar-Månsson B 1994 Mineral distribution in the enamel of teeth with amelogenesis imperfecta as determined by quantitative microradiography. Scand J Dent Res 102:193-197
7. Bäckman B, Anneroth G 1989 Microradiographic study of amelogenesis imperfecta. Scand J Dent Res 97:316-329
8. Bäckman B, Holm A-K 1986 Amelogenesis imperfecta: prevalence and incidence in a northern Swedish county. Community Dent Oral Epidemiol 14:43-47
9. Bäckman B, Anneroth G, Hörstedt P 1989 Amelogenesis imperfecta: a scanning electron microscopic and microradiographic study. J Oral Pathol 18:140-145
10. Bäckman B, Lundgren T, Engström UE et al 1993 The absence of correlations between a clinical classification and ultrastructural findings in amelogenesis imperfecta. Acta Odontol Scand 51:79-89
11. Chosack A, Eidelman E, Wisotsky I, Cohen T 1979 Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta. Oral Surg 47:148-156
12. Escobar VH, Goldblatt LI, Bixler D 1981 A clinical, genetic and ultrastructural study of snow-capped teeth: amelogenesis imperfecta, hypomaturation type. Oral Surg 52:607-614
13. Forsman K, Lind L, Bäckman B, Westermark E, Holmgren G 1994 Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q. Hum Mol Genet 3:1621-1625
14. Kärrman C, Bäckman B, Holmgren G, Forsman K 1996a Genetic heterogeneity of autosomal dominant (ADAI): exclusion from the ADAI region on human chromosome 4q. Arch Oral Biol, in press
15. Kärrman C, Bäckman B, Dixon M, Holmgren G, Forsman K 1996b Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 5 Mb YAC contig on chromosome 4q11-q21. Genomics, submitted
16. Lagerström M, Dahl N, Iselius L, Bäckman B, Pettersson U 1990 Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysis. Am J Hum Genet 46:120-125
17. Lagerström M, Dahl N, Nakahori Y et al 1991 A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1). Genomics 10:971-975
18. Lagerström-Fermér M, Nilsson M, Bäckman B et al 1995 Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta. Genomics 26:159-162
19. Lau EC, Mohandas TK, Shapiro LJ, Slavkin HC, Snead ML 1989 Human and mouse amelogenin loci are on the sex chromosomes. Genomics 4:162-168
20. Lench NJ, Winter GB 1995 Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1). Hum Mutat 5:251-259
21. Lench NJ, Brook AH, Winter GB 1994 SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1). Hum Mol Genet 3:827-828
22. Lyon MF 1961 Gene action in the X-chromosome of the mouse Mus musculus L. Nature 190:372-373
23. Persson M, Sundell S 1982 Facial morphology and open bite deformity in amelogenesis imperfecta. A roentgenocephalometric study. Acta Odontol Scand 40:135-144
24. Pindborg JJ 1982 Aetiology of developmental enamel defects not related to fluorosis. Int Dent J 32:123-134
25. Rowley R, Hill FJ, Winter GB 1982 An investigation of the association between anterior open bite and amelogenesis imperfecta. Am J Orthod 81:229-235
26. Salido EC, Yen PH, Koprivnikar K, Yu L-C, Shapiro LJ 1992 The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes. Am J Hum Genet 50: 303-316
27. Sauk JJ Jr, Vickers RA, Copeland JS, Lyon HW 1972a The surface of genetically determined hypoplastic enamel in human teeth. Oral Surg 34:60-68
28. Sauk JJ Jr, Lyon HW, Witkop CJ Jr 1972b Electron optic microanalysis of two gene products in enamel of females heterozygous for X-linked hypomaturation amelogenesis imperfecta. Am J Hum Genet 24:267-276
29. Sundell S, Valentin J 1986 Hereditary aspects and classification of hereditary amelogenesis imperfecta. Community Dent Oral Epidemiol 14:211-216
30. Winter GB, Brook AH 1975 Enamel hypoplasia and anomalies of the enamel. Dent Clin North Am 19:3-24
31. Witkop CJ Jr 1989 Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol 17:547-553
32. Witkop CJ Jr, Sauk JJ Jr 1976 Heritable defects of enamel. In: Stewarts RE, Prescott GH (eds) Oral facial genetics. Mosby, St Louis, MO, p 151-226
33. Wright JT, Robinson C, Kirkham J 1992 Enamel protein in the different types of amelogenesis imperfecta. In: Slavkin HC, Price PA (eds) The chemistry and biology of mineralized tissues. Elsevier, New York, p 441-450