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宾德综合征:文献综述及两例病例的长期随访

Binder syndrome: literature review and long-term follow-up on two cases.

作者信息

McCollum A G, Wolford L M

机构信息

Department of Orthodontics, University of the Witwatersrand, South Africa.

出版信息

Int J Adult Orthodon Orthognath Surg. 1998;13(1):45-58.

PMID:9558535
Abstract

Binder syndrome has a characteristic clinical appearance including midface hypoplasia, flattened nose, convex upper lip, broad philtrum, crescent-shaped nostrils, and a deep fold or fossa between nose and upper lip. The incisors may be in crossbite with overangulation of the maxillary incisors, and a Class III occlusion is common. Radiographic features include small or absent anterior nasal spine, thin labial plate over incisor roots, nasomaxillary hypoplasia, and skeletal Class III relation. This article reviews the literature in reference to Binder syndrome and presents two patients treated by two different techniques with long-term follow-up. The first patient was treated with traditional orthognathic procedures, whereas the second was treated with a growth-center implant to the nose and orthodontics to treat the occlusion.

摘要

宾德综合征具有特征性的临床表现,包括面中部发育不全、鼻梁扁平、上唇凸出、人中宽阔、新月形鼻孔,以及鼻与上唇之间的深皱襞或凹陷。门牙可能呈反咬合,上颌门牙过度倾斜,Ⅲ类咬合很常见。影像学特征包括前鼻棘小或缺失、门牙牙根上方唇板薄、鼻上颌发育不全以及骨骼Ⅲ类关系。本文回顾了关于宾德综合征的文献,并介绍了两名采用两种不同技术治疗并长期随访的患者。第一名患者采用传统正颌手术治疗,而第二名患者则采用鼻部生长中心植入物及正畸治疗咬合问题。

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