摘要
目的分析遗传性乳光牙本质的特殊临床表现并讨论其发病机制。方法追踪报告1例患儿遗传性乳光牙本质家系,结合相关文献复习。结果本例幼儿属症状较重的遗传性乳光牙本质,其家系中共有7人罹患遗传性乳光牙本质。结论遗传性乳光牙本质低龄患者不可姑息观察,应积极对症治疗与综合预防。
Objective To analyze the special elinical character and mechanism of opalescent dentin.Methods A case of opalcsccat dentin was traced and tclated literutures were revicwed.Results Our investigntion confirmed the infant suffered denti nogenesis imperfecta shields type Ⅱ since other six members in the family were involved.Conclusion For the young patients suffering from deminegenesis imperfecia shields type Ⅱ,active treatments to celieve and prevent symptoms must be taken.
出处
《广东牙病防治》
2006年第1期10-12,共3页
Journal of Dental Prevention and Treatment
关键词
遗传性乳光牙本质
幼儿
乳牙
发病机制
Dcntinogenesis impcrfccta shiclds type Ⅱ Infant Deciduous tooth
