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Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

机译:遗传性牙本质疾病:牙本质生成不全和牙本质发育不良

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摘要

The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal dominant genetic conditions characterised by abnormal dentine structure affecting either the primary or both the primary and secondary dentitions. DGI is reported to have an incidence of 1 in 6,000 to 1 in 8,000, whereas that of DD type 1 is 1 in 100,000. Clinically, the teeth are discoloured and show structural defects such as bulbous crowns and small pulp chambers radiographically. The underlying defect of mineralisation often results in shearing of the overlying enamel leaving exposed weakened dentine which is prone to wear.Currently, three sub-types of DGI and two sub-types of DD are recognised but this categorisation may change when other causative mutations are found. DGI type I is inherited with osteogenesis imperfecta and recent genetic studies have shown that mutations in the genes encoding collagen type 1, COL1A1 and COL1A2, underlie this condition. All other forms of DGI and DD, except DD-1, appear to result from mutations in the gene encoding dentine sialophosphoprotein (DSPP), suggesting that these conditions are allelic.Diagnosis is based on family history, pedigree construction and detailed clinical examination, while genetic diagnosis may become useful in the future once sufficient disease-causing mutations have been discovered. Differential diagnoses include hypocalcified forms of amelogenesis imperfecta, congenital erythropoietic porphyria, conditions leading to early tooth loss (Kostmann's disease, cyclic neutropenia, Chediak-Hegashi syndrome, histiocytosis X, Papillon-Lefevre syndrome), permanent teeth discolouration due to tetracyclines, Vitamin D-dependent and vitamin D-resistant rickets.Treatment involves removal of sources of infection or pain, improvement of aesthetics and protection of the posterior teeth from wear. Beginning in infancy, treatment usually continues into adulthood with a number of options including the use of crowns, over-dentures and dental implants depending on the age of the patient and the condition of the dentition. Where diagnosis occurs early in life and treatment follows the outlined recommendations, good aesthetics and function can be obtained.
机译:遗传性牙本质疾病,牙本质生成不全(DGI)和牙本质发育不良(DD)包括一组常染色体显性遗传疾病,其特征是影响主齿或次齿的牙本质结构异常。据报道,DGI的发病率为6,000的1到8,000的1,而DD 1型的发病率为100,000的1。临床上,牙齿变色并放射线显示结构缺陷,例如球根冠和小的牙髓腔。潜在的矿化缺陷通常会导致上覆的釉质剪切,从而使暴露的弱牙本质易于磨损。目前,已认识到DGI的三种亚型和DD的两种亚型,但是当其他原因性突变被发现时,这种分类可能会改变。找到了。 DGI I型具有成骨不全遗传性,最近的遗传研究表明,编码1型胶原,COL1A1和COL1A2的基因中的突变是这种情况的基础。除DD-1外,所有其他形式的DGI和DD似乎是由编码牙本质唾液磷蛋白(DSPP)的基因突变引起的,表明这些情况是等位基因。诊断基于家族史,血统构建和详细的临床检查,而一旦发现足够的致病突变,遗传诊断就可能在将来变得有用。鉴别诊断包括低钙化形式的釉突生成不全,先天性红细胞生成性卟啉症,导致早期牙齿脱落的疾病(Kostmann病,周期性中性粒细胞减少,Chediak-Hegashi综合征,组织细胞增多症X,Papillon-Lefevre综合征),由于四环素引起的永久性牙齿变色,维生素D依赖治疗且抗维生素D的病。治疗包括去除感染或疼痛的根源,改善美观性并保护后牙免于磨损。从婴儿期开始,治疗通常一直持续到成年期,这取决于患者的年龄和牙列状况,包括使用牙冠,覆盖义齿和种植牙等多种选择。如果诊断是在生命早期进行的,并且治疗遵循概述的建议,则可以获得良好的美观和功能。

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