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Severely hypoplastic amelogenesis imperfecta with taurodontism

✍ Scribed by ALENKA PAVLIČ; PIRJO-LIISA LUKINMAA; PEKKA NIEMINEN; ANU KIUKKONEN; SATU ALALUUSUA

Book ID
108829305
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
205 KB
Volume
17
Category
Article
ISSN
0960-7439

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Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects without any other nonoral symptoms. Recently, a disease-causing nonsense mutation (c.406C>T) in a novel gene, FAM20A, was identified in a large consanguineous family affected by AI wit