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Nonsyndromic Familial Oligodontia with Multiple Dens Invaginatus: A Case Report of an Unusual Case

机译:非综合征性家族性多齿畸形少牙症:一例罕见病例的报告。

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摘要

Oligodontia is a rare dental anomaly with a prevalence of 0.3% in permanent teeth and much less frequency in the primary dentition. Familial oligodontia represents an absence of varying numbers of primary and/or secondary teeth as an isolated trait. It is a complex and multifactorial condition. Many explanations—evolutionary, genetic, and environmental—have been proposed as the etiology. Simultaneous with oligodontia are often the different positional changes of the existing teeth, their morphology, size, and growth disturbances of the maxillofacial skeleton. Early recognition is vital to provide adequate treatment and prevent squeal. Multidisciplinary referral or consultation is thus important in treatment planning to improve function and esthetics. The present paper reports a rare case of familial oligodontia associated with multiple dense invaginatus and microdontia.
机译:Oligodontia是一种罕见的牙齿畸形,在恒牙中的患病率为0.3%,在原牙中的患病率要低得多。家族性少牙症代表一种孤立的特征,即不存在数量不等的乳牙和/或继发牙齿。这是一个复杂的多因素条件。作为病因,提出了许多解释,包括进化论,遗传学和环境学。与少牙症同时发生的往往是现有牙齿的不同位置变化,它们的形态,大小以及颌面骨骼的生长障碍。早期识别对于提供适当的治疗和防止尖叫声至关重要。因此,多学科的转诊或咨询对于改善功能和美学的治疗计划很重要。本文报道了一例罕见的家族性少尿症,伴有多发密集的内陷和小牙畸形。

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