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[孤立性上颌中切牙正中综合征]

[Solitary median maxillary central incisor syndrome].

作者信息

Scholtes E, Kawamoto T, Ockeloen C W, Kleefstra T, Carels C E L

出版信息

Ned Tijdschr Tandheelkd. 2014 Sep;121(9):435-42.

Abstract

Solitary Median Maxillary Central Incisor syndrome is a rare condition (prevalence 1:50,000), with the characteristic dental feature of a solitary central incisor in the maxilla, positioned exactly in the midline. This single incisor is symmetrical and can be present in the deciduous as well as in the permanent dentition. The syndrome can occur as a mild form of the broad holoprosencephaly-spectrum, but can also be associated with other characteristics. The etiology is still largely unknown, but the syndrome is probably based especially on genetic causes. Early recognition of the syndrome is of great importance for establishing the diagnosis, for additional investigation, for possible treatment of associated anomalies and for the correct advice concerning the risk of inheritance of severe congenital birth defects, related to holoprosencephaly. Dentists and orthodontists can play an important role in this regard and should therefore be able to recognise the clinical features of this condition and know how to refer a patient for further diagnostic counselling.

摘要

孤立性上颌中切牙综合征是一种罕见病症(患病率为1:50,000),其特征性牙齿表现为上颌出现一颗孤立的中切牙,且恰好位于中线位置。这颗单颗中切牙形态对称,可出现在乳牙列和恒牙列中。该综合征可能是广泛的前脑无裂畸形谱系的一种轻度形式,但也可能与其他特征相关。病因在很大程度上仍不明确,但该综合征可能尤其基于遗传原因。早期识别该综合征对于确立诊断、进行进一步检查、对相关异常情况进行可能的治疗以及就与前脑无裂畸形相关的严重先天性出生缺陷的遗传风险提供正确建议至关重要。在这方面,牙医和正畸医生可发挥重要作用,因此应能够识别该病症的临床特征,并知道如何将患者转介以获得进一步的诊断咨询。

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