Greene Stephen L, Kau Chung How, Sittitavornwong Somsak, Powell Kathlyn, Childers Noel K, MacDougall Mary, Lamani Ejvis
Department of Pediatric.
Institute of Oral Health Research.
J Craniofac Surg. 2018 Jun;29(4):959-965. doi: 10.1097/SCS.0000000000004334.
Cleidocranial dysplasia (CCD, MIM 119600) is a rare autosomal dominant disorder affecting bone, cartilage, craniofacial growth, and tooth formation leading to supernumerary teeth. Few reports delineate the genotype-phenotype correlations related to the variations in craniofacial morphology and patterning of the dentition and the complexity of treating patient's malocclusion. Successful management of the craniofacial deformities in patients with CCD requires a multidisciplinary team of healthcare specialists. Approximately 70% of patients are due to point mutations in RUNX2 and <20% due to copy number variations with the remainder unidentified. There is no literature to date, describing the orthognathic management of CCD patients with deletion in one of the RUNX2 alleles. The purpose of this study was to evaluate the craniofacial morphology and dental patterning in a 14-year-old Caucasian female with CCD resulting from a novel microdeletion of RUNX2 in 1 allele. The CCD patient with RUNX2 haploinsufficiency due to microdeletion had decreased craniofacial bone and ankyloses in the permanent dentition. An altered extraction protocol of supernumerary teeth was followed in this patient. Craniofacial growth and morphologic analysis demonstrated atypical skull shape, persistent metopic suture, and decreased mandibular size.
锁骨颅骨发育不全(CCD,MIM 119600)是一种罕见的常染色体显性疾病,会影响骨骼、软骨、颅面生长和牙齿形成,导致多生牙。很少有报告描述与颅面形态变化、牙列模式以及治疗患者错牙合复杂性相关的基因型-表型相关性。成功管理CCD患者的颅面畸形需要多学科医疗专家团队。大约70%的患者是由于RUNX2的点突变,<20%是由于拷贝数变异,其余原因不明。迄今为止,尚无文献描述RUNX2一个等位基因缺失的CCD患者的正颌治疗。本研究的目的是评估一名14岁白种女性因RUNX2一个等位基因的新型微缺失导致的CCD患者的颅面形态和牙列模式。因微缺失导致RUNX2单倍体不足的CCD患者颅面骨减少,恒牙列出现强直。该患者采用了改变的多生牙拔除方案。颅面生长和形态分析显示颅骨形状不典型、额缝持续存在以及下颌尺寸减小。