Ehlers-Danlos综合征(VIII型)。

A Apaydin
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引用次数: 15

摘要

ehers - danlos综合征(EDS)是一组罕见的常染色体显性遗传结缔组织发育不良,主要以胶原合成异常为特征,已被证明具有广泛的异质性,至少有11种临床实体根据其临床、生化和遗传特征进行区分。其中,从牙科的角度来看,VIII型EDS特别令人感兴趣,主要原因是口腔黏膜和血管的脆弱性,以及导致牙槽骨严重丢失的侵袭性牙周炎;所有这些实体的临床表现使得在牙科治疗过程中有必要进行护理。在这里,我们提出一例EDS VIII型,具有典型的临床表现,以及牙科治疗方式的细节,重点是手术方法。
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Ehlers-Danlos syndrome (type VIII).

Ehlers-Danlos syndrome (EDS), a group of rare, autosomal dominantly inherited connective tissue dysplasias, characterized mainly by abnormal collagen synthesis, has been shown to exhibit extensive heterogeneity with at least 11 clinical entities differentiated by their clinical, biochemical, and genetic features. Of these, Type VIII EDS is of special interest from a dental viewpoint, due mainly to the resulting fragility of the oral mucosa and blood vessels, and an aggressive type of periodontitis causing severe loss of alveolar bone; all of these clinical manifestations of the entity make it necessary to exercise care during the dental treatment procedures. Here we present a case of EDS Type VIII with typical clinical findings, together with details of the dental treatment modalities, placing emphasis on surgical methods.

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