Wiebe C B, Silver J G, Larjava H S
Department of Clinical Dental Sciences, University of British Columbia, Vancouver.
J Periodontol. 1996 Oct;67(10):1004-10. doi: 10.1902/jop.1996.67.10.1004.
Weary-Kindler syndrome is a rare and poorly understood genetic disorder that has manifestations of both epidermolysis bullosa and poikiloderma congenitale. There are approximately 70 cases documented in the past 40 years but no cases appear in the dental literature, although dental findings have been discussed superficially in dermatological and pediatric publications. This case reports on the periodontal findings and treatment for a 16-year-old female diagnosed with the syndrome. Early exfoliation of deciduous teeth, severe periodontal bone loss around many permanent teeth, and fragile bleeding gingiva were key features. Microbiological testing revealed an absence of Actinobacillus actinomycetemcomitans and low levels of other commonly accepted periodontal pathogens. Tests for inflammation, including AST and elastase, were positive prior to therapy and greatly decreased after mechanical root instrumentation. A beneficial effect of non-surgical periodontal therapy was observed in the short-term follow-up.
韦里-金德勒综合征是一种罕见且了解甚少的遗传性疾病,具有大疱性表皮松解症和先天性皮肤异色症的表现。在过去40年中记录了约70例病例,但牙科文献中未见相关病例报道,尽管皮肤病学和儿科学出版物中曾对牙科检查结果进行过简要讨论。本文报告了一名被诊断患有该综合征的16岁女性的牙周检查结果及治疗情况。乳牙早期脱落、多颗恒牙周围严重的牙周骨丧失以及脆弱易出血的牙龈是主要特征。微生物检测显示不存在伴放线放线杆菌,且其他常见的牙周病原体水平较低。治疗前炎症检测(包括谷草转氨酶和弹性蛋白酶)呈阳性,机械性根面清创术后大幅下降。在短期随访中观察到非手术牙周治疗具有有益效果。