Zimmerman-Laband综合征的正畸及外科治疗。

Teleri Perks, Hashmat Popat, Andrew J Cronin, Peter Durning, Roger Maggs
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引用次数: 3

摘要

Zimmermann-Laband综合征(ZLS)是一种罕见的常染色体疾病,其特征为牙龈纤维瘤病、鼻和/或耳异常、手脚指甲或末节指骨发育不全、关节过度伸展、肝脾肿大、多毛和智力残疾。该综合征的特征是高度可变和复杂的。本文报告1例ZLS及其临床表现,并结合文献资料进行分析。综合管理患者的牙列被描述,重点是正畸和手术的考虑,临床医生应该意识到,当治疗患者的综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The orthodontic and surgical management of Zimmerman-Laband syndrome.

Zimmermann-Laband syndrome (ZLS) is a rare autosomal disorder characterized by gingival fibromatosis, abnormalities of the nose and/or ears, hypoplasia of the nails or terminal phalanges of the hands and feet, hyperextensibility of joints, hepatosplenomegaly, hirsutism, and intellectual disability. The characteristics of the syndrome are highly variable and complicated. This paper reports a case of ZLS and the clinical manifestations encountered in relation to the current available literature. The comprehensive management of the patient's dentition is described, focusing on the orthodontic and surgical considerations clinicians should be aware of when treating patients with the syndrome.

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