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Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontism
Author(s) -
Aldred MJ,
Savarirayan R,
Lamandé SR,
Crawford PJM
Publication year - 2002
Publication title -
oral diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.953
H-Index - 87
eISSN - 1601-0825
pISSN - 1354-523X
DOI - 10.1034/j.1601-0825.2002.1c766.x
Subject(s) - amelogenesis imperfecta , dentition , medicine , permanent dentition , orthodontics , phenotype , dentistry , enamel paint , genetics , biology , gene
This paper describes the clinical features of a family of four generations with autosomal dominant amelogenesis imperfecta with taurodontism (ADAIT). Considerable variation in phenotype was seen, both between individuals and within the dentition of some individuals. Many of the adults had received extensive dental restorative work. These findings re‐enforce previous observations of variable phenotype in this and other forms of the condition and add to the argument for a revision of methods of classification. This history of this large family draws further attention to the restorative demands of this group of dental anomalies and, by their generous co‐operation, will prove an invaluable help in the investigation by molecular genetic techniques of this disfiguring condition.