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迷你种植体辅助腭扩张术和交界性大疱性表皮松解症与釉质发育不全的数字化设计:病例报告。

Mini-implant assisted palate expansion and digital design in junctional epidermolysis bullosa and amelogenesis imperfecta: Case report.

机构信息

Special Care Dentistry Unit, Facultad de Odontología, Universidad de Chile, Santiago, Chile.

Facultad de Medicina y Odontología, Universidad de Santiago de Compostela, Santiago de Compostela, Spain.

出版信息

Spec Care Dentist. 2024 Nov-Dec;44(6):1572-1580. doi: 10.1111/scd.13044. Epub 2024 Jul 21.

Abstract

BACKGROUND

Junctional epidermolysis bullosa (JEB) is one of the four major types of EB caused by genetic variants in the genes coding the proteins of the lamina lucida. All patients with this major type of EB present syndromic hypoplastic amelogenesis imperfecta (AI), with either a pits and fissures or generalized hypoplastic phenotype. Severe forms of AI are associated with compromised oral health-related quality of life (QoL) mostly due to poor dental aesthetics, dentofacial anomalies, and oral pain.

AIM

To present the comprehensive dental treatment of a patient with JEB and AI from the age of 20 months until the age of 18 years, including complex orthodontics and digital oral rehabilitation.

MATERIALS AND METHODS

A male patient with intermediate JEB (homozygous c.3228+1G>A LAMB3 variant) has been under the care of the special care dentistry clinic of the University of Chile since the age of 20 months. His complex dental needs include structural enamel abnormalities in primary and permanent dentition (hypoplastic generalized AI), severe dental crowding with maxillary compression, Class III skeletal pattern, agenesia (#45), and gingivitis.

RESULTS

Pediatric dental care included oral hygiene education and preventive strategies (prophylaxis and fluoride applications), maintaining the dentition free of caries. Due to AI, severe tooth sensitivity hindered proper oral hygiene and required early rehabilitation with temporary polycarbonate and metallic crowns. At the age of 16, the patient began orthodontic treatment. A maxillary expansion was performed with two consecutive mini-implant assisted rapid palate expansion (MARPE) bonded to four mini-implants in the palate. After finishing orthodontic treatment metallic multibrackets (duration 19 months), a definitive oral rehabilitation based on digital smile design with feldspathic crowns of all anterior teeth and premolars was performed.

CONCLUSION

Patients with severe generalized hypoplastic syndromic AI associated with JEB benefit from long-term preventive oral care. Complex orthodontic techniques, such as MARPE, and multibrackets can be successfully. Digital smile design provides a definitive oral rehabilitation technique improving oral function, aesthetics, and QoL.

摘要

背景

交界型大疱性表皮松解症(JEB)是由编码板层素 lucida 蛋白的基因突变引起的四种 EB 主要类型之一。所有此类主要类型 EB 患者均表现出综合征性牙釉质发育不全(AI),表现为窝沟或广泛的牙体形态发育不全。严重的 AI 与口腔健康相关的生活质量受损(QoL)有关,主要是由于较差的牙齿美观、牙颌面畸形和口腔疼痛。

目的

介绍一位 JEB 和 AI 患者从 20 个月龄到 18 岁的综合牙科治疗,包括复杂的正畸和数字化口腔修复。

材料和方法

一位中间型 JEB (纯合子 c.3228+1G>A LAMB3 变体)患者自 20 个月龄起一直在智利大学特殊护理牙科诊所接受治疗。他的复杂牙科需求包括乳牙和恒牙的结构釉质异常(广泛性牙釉质发育不全)、上颌压缩导致的严重牙齿拥挤、III 类骨骼模式、缺牙(#45)和牙龈炎。

结果

儿科牙科护理包括口腔卫生教育和预防策略(预防和氟化物应用),保持无龋状态。由于 AI,严重的牙齿敏感妨碍了适当的口腔卫生,需要早期用临时聚碳酸酯和金属冠修复。16 岁时,患者开始接受正畸治疗。上颌采用连续两次微型植入物辅助快速腭扩张(MARPE)治疗,在上颌腭部粘结四颗微型植入物。完成正畸治疗后(19 个月),使用基于数字化微笑设计的长石冠对所有前牙和前磨牙进行了最终的口腔修复。

结论

与 JEB 相关的严重广泛性牙釉质发育不全综合征患者受益于长期预防性口腔护理。MARPE 等复杂正畸技术和多弓丝技术可以成功应用。数字化微笑设计提供了一种最终的口腔修复技术,可以改善口腔功能、美观和 QoL。

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