遗传性乳光牙本质病例追踪报告  

A Case Report of Dentinogenesis Imperfecta Shields Type Ⅱ and Literature Review

作　　者：任飞[1] 叶小雅[1] 仇金泉[1] 李海群[1] 詹捷玲[1] 

机构地区：[1]广东省口腔医院.南方医科大学附属口腔医院儿童牙科,广东广州510280

出　　处：《广东牙病防治》2006年第1期10-12,共3页Journal of Dental Prevention and Treatment

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.

关 键 词：遗传性乳光牙本质 幼儿 乳牙 发病机制 

分 类 号：R781.2[医药卫生—口腔医学] R512.62[医药卫生—临床医学]