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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Dentinogenesis Imperfecta: A Family which was Affected for Over Three Generations
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Dentinogenesis Imperfecta: A Family which was Affected for Over Three Generations

机译：牙本质生成不全：受影响的家族超过三代

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摘要

Dentinogenesis Imperfecta (DI) or hereditary opalescent dentin is inherited in a simple autosomal dominant mode with high penetrance and low mutation rates. It generally affects both the deciduous and the permanent dentitions. DI corresponds to a localized form of mesodermal dysplasia which is observed in the histo-differentiation. An early diagnosis and treatment are therefore fundamental, which aim at obtaining a favourable prognosis, since at late intervention makes the treatment more complex. We are presenting here a case of DI in which the disease affected the three generations of a family in India.
机译：牙本质生成不全症（DI）或遗传性乳白色牙本质以简单的常染色体显性遗传方式遗传，具有高渗透率和低突变率。它通常影响落叶和永久牙列。 DI对应于在组织分化中观察到的中胚层发育异常的局部形式。因此，早期诊断和治疗是基本的，其目的是获得良好的预后，因为在晚期进行干预会使治疗更加复杂。我们在这里介绍一个DI病例，其中该病影响了印度三代家庭。

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