Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontism

Oral Diseases

Volumn 8, Issue 1, 2002, Pages 62-68

  Aldred, M J ^a,b,c   Savarirayan, R ^a,b,c   Lamande S R ^b,c   Crawford, P J M ^d  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

^b MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^c UNIVERSITY OF MELBOURNE   (Australia)

^d UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

Amelogenesis imperfecta; Genetic; Taurodontism, enamel

Indexed keywords

ADOLESCENT; AMELOGENESIS IMPERFECTA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; DISEASE CLASSIFICATION; DISEASE COURSE; FEMALE; GENETIC ANALYSIS; HUMAN; MALE; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; TAURODONTISM; TOOTH DISEASE; TOOTH RADIOGRAPHY;

ADOLESCENT; ADULT; AMELOGENESIS IMPERFECTA; CHILD; DENTAL PULP; FEMALE; GENES, DOMINANT; HUMANS; INCISOR; MALE; ODONTOMETRY; PEDIGREE; PHENOTYPE; TOOTH DISCOLORATION; TOOTH ROOT; VICTORIA;

EID: 0036121405     PISSN: 1354523X     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1601-0825.2002.1c766.x     Document Type: Article

References (24)

1. Variable expression in amelogenesis imperfecta with taurodontism
2. Ameliogenesis imperfecta-towards a new classification
3. Amelogenesis imperfecta: A genetic Study
4. Amelogenesis imperfecta with taurodontism
5. Concomitant taurodontism and amelogenesis imperfecta in the American Caucasian
6. Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: Separate conditions or a spectrum of disease?
7. Amelogenesis imperfecta: Autosomal dominant hypomaturation-hypoplasia type with taurodontism
8. Tricho-dento-osseous syndrome
9. Genetic linkage of the tricho-dento-osseous syndrome to chromosome 17q21
10. Dental abnormalities in the tricho-dento-osseous syndrome
11. The tricho-dento-osseous syndrome
12. Tricho-dento-osseous syndrome: A scanning electron microscopic analysis
13. Tricho-dento-osseous syndrome
14. A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families
15. Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
16. Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions
17. Clinical heterogeneity in the tricho-dento-osseous syndrome
18. Hereditary enamel hypoplasia, its association with characteristic hair structure
19. Taurodontism of the mandibular first permanent molar distinguishes between the tricho-dento-osseous (TDO) syndrome and amelogenesis imperfecta
20. Tricho-dento-osseous syndrome: Heterogeneity or clinical variability
21. Hereditary amelogenesis imperfecta. A rare autosomal dominant type
22. Analysis of the tricho-dento-osseous syndrome genotype and phenotype
23. Tricho-dento-osseous syndrome. Features of the hair and teeth