ICD-11 编码查询_国际疾病分类第 11 版中文版_在线疾病编码检索工具
LA30.6

遗传性釉质发育不全

Amelogenesis imperfecta

上级条目
LA30 牙和牙周组织结构发育异常
层级
5 级

定义

釉质发育不全表现为牙釉质或牙冠外层的罕见异常形成。釉质发育不全是由于釉质中的蛋白质:成釉蛋白、釉蛋白、釉丛蛋白和釉原蛋白的功能紊乱所致。患釉质发育不全患者的牙齿颜色异常:黄色、棕色或灰色;这种疾病可影响两牙列的任意数量的牙齿。牙齿患龋齿的风险较高,对温度变化、快速磨损、牙结石过度沉积和牙龈增生都很敏感。

Amelogenesis imperfecta presents with a rare abnormal formation of the enamel or external layer of the crown of teeth. Amelogenesis imperfecta is due to the malfunction of the proteins in the enamel: ameloblastin, enamelin, tuftelin and amelogenin. People afflicted with amelogenesis imperfecta have teeth with abnormal colour: yellow, brown or grey; this disorder can afflict any number of teeth of both dentitions. The teeth have a higher risk for dental cavities and are hypersensitive to temperature changes as well as rapid attrition, excessive calculus deposition, and gingival hyperplasia.

包含词 该编码包含的临床情况,通常不作为独立编码

  • 釉质矿化不良型遗传性釉质发育不全
  • 釉质未成熟型遗传性釉质发育不全
英文词条(2)
  • Hypocalcified amelogenesis imperfecta
  • Hypomaturation amelogenesis imperfecta

索引词 可用于检索该条目的同义词与别名

  • 遗传性釉质发育不全
  • AI[遗传性釉质发育不全]
  • 釉质矿化不良型遗传性釉质发育不全
  • 矿化减少遗传性釉质发育不全
  • 釉质未成熟型遗传性釉质发育不全
  • 釉质未成熟釉质发育不良型遗传性釉质发育不全伴牛牙症
  • 釉质发育不良型遗传性釉质发育不全
  • 发育不良性遗传性釉质发育不全
  • 遗传性釉质发育不全
  • 先天性釉质发育不全
  • 遗传性釉质发育不全-牙龈增生
  • 遗传性釉质发育不全-锥杆营养不良
  • Jalili综合征
  • 遗传性釉质发育不全-肾钙质沉着症
英文词条(14)
  • Amelogenesis imperfecta
  • AI - [amelogenesis imperfecta]
  • Hypocalcified amelogenesis imperfecta
  • hypomineralisation amelogenesis imperfecta
  • Hypomaturation amelogenesis imperfecta
  • Hypomaturation hypoplastic amelogenesis imperfecta with taurodontism
  • Hypoplastic amelogenesis imperfecta
  • congenital enamel hypoplasia
  • hereditary enamel hypoplasia
  • hypoplasia amelogenesis imperfecta
  • Amelogenesis imperfecta - gingival hyperplasia
  • Amelogenesis imperfecta - cone rod dystrophy
  • Jalili syndrome
  • Amelogenesis imperfecta - nephrocalcinosis

后组配轴 Postcoordination

该条目未定义后组配轴,直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式,不是必填项。