Dentinogenesis imperfecta type II: an affected family saga

• Kamboj Mala

  Department of Oral Pathology and Microbiology, U.P. King George's University of Dental Sciences

• Chandra Anil

  Department of Operative Dentistry, U.P. King George's University of Dental Sciences

抄録

Dentinogenesis imperfecta (DI) type II or hereditary opalescent dentin is inherited in simple autosomal dominant mode with high penetrance and low mutation rate. It generally affects both the deciduous and permanent dentitions. DI type II corresponds to a localized form of mesodermal dysplasia, observed in histodifferentiation. Early diagnosis and treatment are therefore, fundamental, aiming at obtaining a favourable prognosis since late intervention makes treatment more complex. We present two cases of DI type II with the disease affecting three generations of a family in India, and briefly highlight the molecular basis of this disease. (J. Oral Sci. 49, 241-244, 2007)

収録刊行物

• Ｊｏｕｒｎａｌ　ｏｆ　Ｏｒａｌ　Ｓｃｉｅｎｃｅ

  Ｊｏｕｒｎａｌ　ｏｆ　Ｏｒａｌ　Ｓｃｉｅｎｃｅ 49 (3), 241-244, 2007

  日本大学歯学部

キーワード

• dentinogenesis imperfecta
• type II
• dentin
• permanent dentition

詳細情報

• CRID: 1390001205045282432
• NII論文ID: 130000072677
• DOI: 10.2334/josnusd.49.241
• ISSN: 18804926
• ISSN: 13434934
• Web Site: https://www.jstage.jst.go.jp/article/josnusd/49/3/49_3_241/_pdf
• Web Site: https://search.jamas.or.jp/link/ui/2008170709
• 本文言語コード: en
• データソース種別:
  • JaLC
  • Crossref
  • CiNii Articles
• 抄録ライセンスフラグ: 使用不可