Lukinmaa P L, Ranta H, Ranta K, Kaitila I, Hietanen J
J Craniofac Genet Dev Biol. 1987;7(2):127-35.
Orthopantomograms of 49 patients with osteogenesis imperfecta (OI) classified according to Sillence were examined for dysplastic dentin defects and other developmental abnormalities of the teeth. Thistle-tube-shaped pulps in the permanent teeth were observed in five patients. Four of them had pulp stones in several teeth. Apically extended pulp chambers were present in 3/49 patients, and the structure of the mandible was cystic in 1/49. These defects occurred in patients with type I or unclassifiable OI and were mainly not associated with type I dentinogenesis imperfecta (DI). The prevalence rates of invaginations (10.2%) and hypodontia of permanent teeth (18.4%) exceeded those in the normal population. The frequent developmental disturbances of the teeth in OI may be secondary to the connective tissue defect. The relation of the dysplastic defects other than type I DI to OI remains to be clarified.
对49例根据席伦斯分类法分类的成骨不全(OI)患者的曲面体层片进行检查,以观察发育异常的牙本质缺陷和其他牙齿发育异常情况。在5例患者中观察到恒牙呈蓟管状牙髓。其中4例患者的几颗牙齿中有牙髓石。49例患者中有3例存在根尖部扩展的髓腔,49例中有1例下颌骨结构呈囊性。这些缺陷发生在I型或无法分类的OI患者中,主要与I型牙本质发育不全(DI)无关。恒牙内陷(10.2%)和恒牙先天缺牙(18.4%)的患病率超过正常人群。OI中牙齿频繁出现的发育障碍可能继发于结缔组织缺陷。I型DI以外的发育异常缺陷与OI的关系仍有待阐明。