交界性表皮松解症和成骨不全症的微型植入物辅助腭扩张和数字化设计:病例报告。

IF 0.9 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
Special Care in Dentistry Pub Date : 2024-11-01 Epub Date: 2024-07-21 DOI:10.1111/scd.13044
Sebastian Véliz, Antonio Olivares, Susanne Krämer
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引用次数: 0

摘要

背景:交界性表皮松解症(JEB)是由编码透明层蛋白的基因变异引起的四大类 EB 之一。所有这种主要类型的 EB 患者都表现为综合征性发育不全髓质发育不全(AI),具有凹陷和裂隙或全身发育不全表型。AI 的严重形式与口腔健康相关的生活质量(QoL)受损有关,这主要是由于牙齿美观度差、颌面部异常和口腔疼痛所致:一名患有中度JEB(同基因c.3228+1G>A LAMB3变异体)的男性患者自20个月大起一直在智利大学牙科特殊护理诊所接受治疗。他有复杂的牙科需求,包括原牙和恒牙结构性釉质异常(发育不全的全身性 AI)、严重的牙齿拥挤并伴有上颌骨压迫、III 类骨骼模式、躁狂症(45 号)和牙龈炎:儿童牙科护理包括口腔卫生教育和预防策略(预防和涂氟),以保持牙齿无龋。由于 AI,严重的牙齿敏感妨碍了正确的口腔卫生,需要使用聚碳酸酯和金属临时牙冠进行早期修复。16 岁时,患者开始接受正畸治疗。在腭部的四个微型种植体上粘接了两个连续的微型种植体辅助快速腭部扩张(MARPE),进行了上颌扩张。在完成金属多托槽正畸治疗(疗程 19 个月)后,根据数字化微笑设计对所有前牙和前臼齿进行了长石牙冠的最终口腔修复:结论:伴有 JEB 的严重全身发育不全综合征 AI 患者可从长期口腔预防护理中获益。复杂的正畸技术,如 MARPE 和多托槽,也能取得成功。数字化微笑设计提供了一种明确的口腔康复技术,可改善口腔功能、美观和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mini-implant assisted palate expansion and digital design in junctional epidermolysis bullosa and amelogenesis imperfecta: Case report.

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.

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来源期刊
Special Care in Dentistry
Special Care in Dentistry DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
2.40
自引率
14.30%
发文量
120
期刊介绍: Special Care in Dentistry is the official journal of the Special Care Dentistry Association, the American Association of Hospital Dentists, the Academy of Dentistry for Persons with Disabilities, and the American Society for Geriatric Dentistry. It is the only journal published in North America devoted to improving oral health in people with special needs.
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