Huth K Ch, Paschos E, Sagner T, Hickel R
Department of Restorative Dentistry, Periodontology and Pedodontics, Dental School of the Ludwig-Maximilians-University, Munich, Germany.
Int J Paediatr Dent. 2002 Sep;12(5):316-21. doi: 10.1046/j.1365-263x.2002.00390.x.
Dentinogenesis imperfecta type II, also known as hereditary opalescent dentin, is an isolated inherited condition transmitted as an autosomal dominant trait affecting the primary and permanent dentition. The combined pedodontic-orthodontic management of a 4-year-old child is described. Following orthodontic analysis to encourage a favourable growth outcome, treatment comprised restoration of the primary teeth with stainless steel crowns and composite crowns. Differential diagnosis and alternative therapies, including orthodontic considerations, are discussed.
II型牙本质发育不全，也称为遗传性乳光牙本质，是一种孤立的遗传性疾病，以常染色体显性特征遗传，影响乳牙列和恒牙列。本文描述了一名4岁儿童的儿科正畸联合治疗。在进行正畸分析以促进良好的生长结果之后，治疗包括用不锈钢冠和复合冠修复乳牙。文中还讨论了鉴别诊断和替代疗法，包括正畸方面的考虑因素。
