Microdontia

Microdontia
  • 文章类型: Journal Article
    局灶性牙髓是一种牙齿异常,其特征是存在单个异常小的前牙或后牙。这篇文章的目的是提供一个最新的综述,对先进的恢复性管理的焦点微型的文献,并记录了一个临床病例,其中采用了经过审查的先进修复方法来治疗表现为非综合征性不对称局灶性微血管的年轻成年人。我们对现有文献进行了初步研究,以对局灶性微型牙体进行高级修复管理。此外,我们提出了一种微创方法来治疗一名18岁女性患者,该患者患有非综合征性不对称局灶性微血管炎.粘合剂牙科的主要优点是它可以更好地保留较小牙齿的结构。文献综述显示,关于口腔上颌前区局部微小牙体的报道很少。然而,新颖的微创修复程序可以满足患者的美学和功能偏好。执行良好的添加剂诊断蜡和口内模型可以作为永久的修复蓝图,为美学区域的局部牙齿异常提供可预测的结果。总之,在年轻的局灶性牙髓组织患者中使用微创牙科方法可以获得长期满意的美学结果。
    Focal microdontia is a dental anomaly characterized by the presence of a single abnormally small anterior or posterior tooth. The objective of this article is to provide an updated review of the literature on the advanced restorative management of focal microdontia, and to document a clinical case where the reviewed advanced restorative approaches were applied to treat a young adult presenting with a non-syndromic asymmetrical focal microdontia.We conducted a preliminary examination of the existing literature on the advanced restorative management of focal microdontia. Additionally, we presented a minimally invasive approach to the treatment of an 18-year-old female patient with non-syndromic asymmetrical focal microdontia. The primary advantage of adhesive dentistry is that it can better preserve the structure of smaller teeth. A review of literature reveals a paucity of reports on localized microdontia in the maxillary anterior region of the mouth. However, novel minimally invasive restorative procedures satisfy patients\' aesthetic and functional preferences. Well-executed additive diagnostic wax-ups and intraoral mock-ups can serve as a permanent restoration blueprint, providing predictable results for focal dental anomalies in the aesthetic zone. In conclusion, the use of minimally invasive dental approaches in young patients with focal microdontia can result in long-term satisfactory aesthetic outcomes.
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  • 文章类型: Case Reports
    Weyers肩面骨发育不良(WAD)是一种罕见的骨骼发育不良,是常染色体显性遗传,临床症状表现为牙齿异常,多指,指甲营养不良,身材矮小。它也被称为“Curry-Hall综合征”,据报道与染色体4p16上的基因突变有关,据报道该区域通常与类似的遗传综合征有关。Ellis-vanCreveld(EVC)综合征。大多数EVC患者患有先天性心脏异常,最常见的是房间隔缺损,不像WAD。在这种情况下,一名15岁的女孩出现甲营养不良,手脚多指,microdontia,或者牙齿发育不全,呈圆锥形,身材矮小.病人从出生起就有指甲营养不良,身高方面的身体生长与年龄方面的正常生长参数不匹配。患者也有锥形牙齿的异常凹陷,其余临床表现提示WAD。
    Weyers acrofacial dysostosis (WAD) is a rare skeletal dysplasia, which is autosomal-dominant, and the clinical symptoms are presented as dental anomalies, polydactyly, nail dystrophy, and short physical stature. It is also termed \"Curry‑Hall syndrome\" and reported to be linked to genetic mutations mapped on chromosome 4p16, the region reported being commonly associated with a similar genetic syndrome, Ellis-van Creveld (EVC) syndrome. Most individuals with EVC have congenital heart abnormalities, most often atrial septal defects, unlike WAD. In this case, a 15‑year‑old girl presented with onychodystrophy and polydactyly observed in the hands and feet, microdontia, or agenesis of teeth, which were conical in shape, with a short stature. The patient had dystrophy of nails since birth, and physical growth in terms of height did not match the normal growth parameters with respect to age. The patient also had abnormal dentation with conical-shaped teeth, with the rest of the clinical presentations suggestive of WAD.
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  • 文章类型: Case Reports
    Restorative treatment of microdontia teeth is often considered as the final step of post-orthodontic treatment. Based on digital workflow, this clinical report presents pre-orthodontic reshaping of anterior teeth in the smile disharmony of a young patient using bilayering composite injection technique. Transparent silicone indexes for dentin and enamel fillings were fabricated from three-dimensional-printed models of the digital wax-up. This noninvasive, simple and straightforward injection technique was able to provide semipermanent reversible aesthetic restorations while awaiting for adulthood and definitive prosthodontic solution. Closure of diastemas before orthodontic treatment were carried out to restore functional contact point and to guide future teeth movements.
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  • 文章类型: Case Reports
    儿科美学牙科是一种敏感的技术,因为孩子们可能不太合作;因此,最低限度的任命是首选。前美学康复最保守的治疗方式是使用直接复合贴面修复。在许多情况下,在儿科患者的生长阶段完成之前,使用复合树脂改善美学是唯一可能的选择。在这篇文章中,我们在需要美学修复的不同治疗需求的青少年中提出了三种不同的情况。首例病例报告是一位牙釉质发育不全患者,第二个是广义间距,第三个是局部的microdontia。所有三名患者在直接复合贴面后随访六个月,对他们的治疗结果非常满意。这增强了他们的自信心。
    Pediatric esthetic dentistry is a sensitive technique, as children can be less cooperative; hence, minimal appointments are preferred. The most conservative treatment modality for anterior esthetic rehabilitation is using direct composite veneer restorations. In many instances, esthetic improvements using composite resin are the only possible option until the growth phase of the pediatric patient is complete. In this article, we present three different case scenarios in young teenagers with different treatment needs requiring esthetic restorations. The first case report is a patient with amelogenesis imperfecta, the second is with generalized spacing, and the third is with localized microdontia. All three patients were followed up for six months post direct composite veneering and were highly satisfied with their treatment outcomes, which boosted their self-confidence.
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  • 文章类型: Case Reports
    Fontaineprogeroid综合征(FPS)是由SLC25A24基因的致病变异引起的常染色体显性疾病。文献中描述了11例,有些人具有早期杀伤力。我们讨论了患者从出生到7个月死亡的临床过程。
    Fontaine progeroid syndrome (FPS) is an autosomal dominant condition caused by pathogenic variants in the SLC25A24 gene. Eleven cases have been described in the literature, with early lethality in some. We discuss the clinical course of a patient from birth until his death at 7 months.
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  • 文章类型: Case Reports
    对儿科患者尤其是3岁以下的患者使用的化学疗法会导致牙齿发育障碍。此病例报告的目的是介绍在早期接受间变性室管膜瘤(WHOIII)治疗的患者中化疗的晚期牙齿效应。9岁时的影像学发现显示六颗牙齿的少突,上颌侧切牙,上颌和下颌第一前磨牙。化疗后的儿科癌症幸存者患一种或多种牙齿发育障碍的风险增加。确保适当的牙齿护理并评估对口腔健康的长期影响,牙齿发育,和遮挡,牙医的参与至关重要。对牙齿缺损进行充分的诊断和有计划的治疗可以显着改善患者口腔健康相关的生活质量。
    Chemotherapy used on pediatric patients especially those below 3 years of age causes disturbances in dental development. The aim of this case report was to present the late dental effects of chemotherapy in a patient treated for anaplastic ependymoma (WHO III) at an early age. Radiographic findings at the age of 9 years showed oligomicrodontia of six teeth, maxillary lateral incisors, and maxillary and mandibular first premolars. Pediatric cancer survivors after chemotherapy have an increased risk of one or more dental development disorders. To ensure proper dental care and to assess the long-term effects on oral health, tooth development, and occlusion, the involvement of a dentist is crucial. Adequate diagnosis and well-planned treatment of the dental defect can significantly improve patient oral health-related quality of life.
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  • 文章类型: Case Reports
    Oral rehabilitation of patients presenting multiple microdontia is a real therapeutic challenge. These alterations in size, often associated with other dental anomalies, have aesthetic and functional repercussions for patients and can lead to significant psycho-social consequences. We report here the case of an 11-year-old patient with bilateral sectorial microdontia and agenesis of teeth numbers 13 and 23. She also presented staturo-ponderal delay and a history of acute coronary syndrome with a lower coronary occlusion of unknown aetiology. At first, additive coronoplasties and an orthodontically retained interim prosthesis answered the aesthetic and functional need during childhood and adolescence. Once she reached adulthood, a multidisciplinary meeting was conducted and a treatment plan was established. The decision was made to rehabilitate the upper arch with a permanent bridge and the lower arch with indirect adhesive restorations. This solution solved the problem of the bilateral lateral infraocclusions and tooth agenesis, restoring both aesthetics and function. This paper presents 15 years of management and treatment of a patient presenting multiple microdontia associated with hypodontia. Both the multidisciplinary approach and coordination between the different medical team members was essential to maintain the existing dentition while preparing, planning, and carrying out a personalized treatment plan once maxillofacial growth was complete.
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  • 文章类型: Case Reports
    Tooth agenesis is a type of dental anomaly in which individuals are missing teeth due to developmental failure as a result of genetic or environmental factors. With approximately one fourth of the population missing ≥1 third molar, tooth agenesis is considered a common dental anomaly. However, the severity of tooth agenesis can range from a missing single tooth to multiple teeth. When suffering from severe tooth agenesis, the patient\'s health and social relationships are often affected.
    The patient in this report congenitally lost 11 teeth and suffered from compromised esthetics and impaired chewing function. In such a severe tooth agenesis case, interdisciplinary treatments involving orthodontics, periodontics, and prosthodontics were engaged to reconstruct the ideal biology, function, and esthetics for the patient. With an interdisciplinary approach, the periodontist played an important role in the rehabilitation of the edentulous regions with implants in combination with various hard and soft tissue augmentation procedures. In addition, the patient with severe tooth agenesis presented with additional dental anomalies. The periodontist, therefore, had to collaborate with other specialists to provide early detection and intervention to avoid future complications, such as the management of infraoccluded ankylosed deciduous molars and aberrant frenum. The patient at the end of treatment had a good occlusion with improved function and esthetics.
    This case report describes the interdisciplinary treatment approach used and points out the role of periodontists in the treatment of a patient with severe tooth agenesis.
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  • 文章类型: Case Reports
    Microdontia is a term used to describe teeth which are smaller than normal. Peg-shaped teeth are type of microdontia, a developmental disturbances of teeth mainly due to congenital reasons. Most commonly affecting single teeth, that is maxillary lateral incisors. Incidence of peg shaped tooth in maxillary laterals are usually seen and reported. But in mandibular arch it is very rare. Present case, it affected all the incisors of mandibular arch and also the laterals of maxillary arch which is rarest of condition. This case report presents a non syndromic, peg shaped mandibular incisors in a 11 year old male patient.
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  • 文章类型: Case Reports
    Oral physician has always been challenged when it comes to diagnosing rare nonsyndromic cases because of the varied presentation of multiple dental abnormalities caused due to mutations in developmental regulatory genes. This coupled with skeletal abnormalities makes the task more difficult. But as we come across such rare constellation of findings, it makes the field more intriguing. Here, we report an extremely rare case of non syndromic occurrence of dental manifestations like multiple dens invaginatus, generalised microdontia, generalised hypoplasia, hypodontia, pulp stones and widening of pulp chamber along with skeletal findings of bilateral syndactyly of legs and brachydactyly of hands and legs. Although many non syndromic cases have been reported in the literature, the unusual occurrence of findings in the present case is being reported for the first time.
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