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加德纳综合征一例的临床特征及其对口腔修复治疗的影响

The clinical features and their impact on the prosthodontic management in a case of Gardner's syndrome.

作者信息

Cunliffe S, Milosevic A

出版信息

Eur J Prosthodont Restor Dent. 2014 Mar;22(1):7-10.

Abstract

Gardner's syndrome is a variant of Familial Adenomatous Polyposis (FAP), a condition that manifests as hundreds of colorectal polyps likely to undergo malignant change by the fourth decade. Early diagnosis of this condition has the potential to be life saving for individuals and due to its inherited nature other family members can often also be affected. Additional features of Gardner's Syndrome include multiple jaw osteomas with missing teeth that can make prosthodontic treatment a challenge. This case report highlights the presenting features and the prosthodontic problems faced when treating a patient with Gardner's syndrome.

摘要

加德纳综合征是家族性腺瘤性息肉病(FAP)的一种变体,这种疾病表现为数百个结直肠息肉,到40岁时很可能发生恶变。早期诊断这种疾病有可能挽救患者生命,而且由于其遗传性,其他家庭成员通常也会受到影响。加德纳综合征的其他特征包括多个颌骨骨瘤和牙齿缺失,这会给口腔修复治疗带来挑战。本病例报告重点介绍了一名加德纳综合征患者的临床表现以及在治疗过程中面临的口腔修复问题。

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