Jasmin J R, Clergeau-Guerithault S
Oral Surg Oral Med Oral Pathol. 1984 Jul;58(1):57-63. doi: 10.1016/0030-4220(84)90365-7.
Dentin dysplasia type II is a rare autosomal dominant defect which affects dentin formation in both the deciduous and the permanent dentitions. The scanning electron microscopic study performed on a primary central incisor presents some findings similar to those reported in dentinogenesis imperfecta. Because of the lack of published reports on dentin dysplasia type II, it is difficult to ascertain definitive characteristics of this dentin abnormality.
II型牙本质发育异常是一种罕见的常染色体显性缺陷，影响乳牙和恒牙的牙本质形成。对一颗乳中切牙进行的扫描电子显微镜研究呈现出一些与牙本质发育不全中所报道的结果相似的发现。由于缺乏关于II型牙本质发育异常的已发表报告，很难确定这种牙本质异常的明确特征。
