Retrouvey Jean-Marc, Taqi Doaa, Tamimi Faleh, Dagdeviren Didem, Glorieux Francis H, Lee Brendan, Hazboun Renna, Krakow Deborah, Sutton V Reid
Faculty of Dentistry, McGill University, Montreal, Quebec, Canada.
Faculty of Dentistry, McGill University, Montreal, Quebec, Canada.
Eur J Med Genet. 2019 Dec;62(12):103606. doi: 10.1016/j.ejmg.2018.12.011. Epub 2018 Dec 26.
Osteogenesis imperfecta (OI) type V is an ultrarare heritable bone disorder caused by the heterozygous c.-14C > T mutation in IFITM5. The oro-dental and craniofacial phenotype has not been described in detail, which we therefore undertook to evaluate in a multicenter study (Brittle Bone Disease Consortium). Fourteen individuals with OI type V (age 3-50 years; 10 females, 4 males) underwent dental and craniofacial assessment. None of the individuals had dentinogenesis imperfecta. Six of the 9 study participants (66%) for whom panoramic radiographs were obtained had at least one missing tooth (range 1-9). Class II molar occlusion was present in 8 (57%) of the 14 study participants. The facial profile was retrusive and lower face height was decreased in 8 (57%) individuals. Cephalometry, performed in three study participants, revealed a severely retrusive maxilla and mandible, and moderately to severly retroclined incisors in a 14-year old girl, a protrusive maxilla and a retrusive mandible in a 14-year old boy. Cone beam computed tomograpy scans were obtained from two study participants and demonstrated intervertebral disc calcification at the C2-C3 level in one individual. Our study observed that OI type V is associated with missing permanent teeth, especially permanent premolar, but not with dentinogenesis imperfecta. The pattern of craniofacial abnormalities in OI type V thus differs from that in other severe OI types, such as OI type III and IV, and could be described as a bimaxillary retrusive malocclusion with reduced lower face height and multiple missing teeth.
V型成骨不全症(OI)是一种极为罕见的遗传性骨病,由IFITM5基因中杂合的c.-14C > T突变引起。口腔-牙齿和颅面表型尚未得到详细描述,因此我们在一项多中心研究(脆性骨病联盟)中对其进行了评估。14名V型OI患者(年龄3至50岁;10名女性,4名男性)接受了牙齿和颅面评估。所有个体均无牙本质发育不全。在获得全景X线片的9名研究参与者中,有6名(66%)至少有一颗牙齿缺失(范围为1至9颗)。14名研究参与者中有8名(57%)存在II类磨牙咬合关系。8名(57%)个体的面部轮廓后缩,面下高度降低。对三名研究参与者进行的头影测量显示,一名14岁女孩上颌骨和下颌骨严重后缩,切牙中度至重度舌倾;一名14岁男孩上颌骨前突,下颌骨后缩。对两名研究参与者进行了锥形束计算机断层扫描,其中一人在C2 - C3水平显示椎间盘钙化。我们的研究观察到,V型OI与恒牙缺失有关,尤其是恒前磨牙,但与牙本质发育不全无关。因此,V型OI的颅面异常模式不同于其他严重的OI类型,如III型和IV型OI,可描述为双颌后缩错牙合,伴有面下高度降低和多颗牙齿缺失。