Int J Stomatol

Inter J Stomatol

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Research actuality of the dentinogenesis imperfecta type Ⅱ

DING Nong-le1, YANG Zheng2, LIU Min1, YANG Si-wei2   

  1. 1. Dept. of Prosthodontics, The Affiliated Hospital of Stomatology, Luzhou Medica
  • Received:2008-05-08 Revised:2009-01-05 Online:2009-03-20 Published:2009-03-20
  • Contact: LIU Min

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Abstract: Dentinogenesis imperfecta type Ⅱ（DGI-Ⅱ）is an autosomal dominant inherited disease. A pathogenesis gene has been located on human chromosome 4q21. At present, the mutations of dentin sialophosphoprotein are one of the reasons of DGI-Ⅱ. This review presented the researches on genetic investigation, inheritance, microscopic anatomy, clinical solutions of dentinogenesis imperfecta type Ⅱ.


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