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一项关于埃勒斯-当洛综合征患者的调查。

A survey of patients with Ehlers-Danlos syndrome.

作者信息

Ainsworth S R, Aulicino P L

机构信息

Department of Orthopaedic Surgery, Eastern Virginia Graduate School of Medicine, Norfolk.

出版信息

Clin Orthop Relat Res. 1993 Jan(286):250-6.

PMID:8425354
Abstract

Ehlers-Danlos syndrome (EDS) is an inherited disorder of collagen biosynthesis. Nine types of the disorder are now recognized. A survey of 151 EDS patients showed a high percentage of the patients were classified as having Types I through IV. Bracing and fusion appear to be the most commonly used methods of orthopedic care. Surgical complications were common. The orthopedist was often the first practitioner to diagnose and treat the patient with EDS. A fundamental understanding of this complex disorder and its varied manifestations is essential to prevent major life-threatening complications.

摘要

埃勒斯-当洛综合征(EDS)是一种遗传性胶原蛋白生物合成障碍疾病。目前已确认该疾病有九种类型。对151例EDS患者的调查显示,有很大比例的患者被归类为患有I型至IV型。支具和融合术似乎是骨科治疗中最常用的方法。手术并发症很常见。骨科医生常常是首位诊断和治疗EDS患者的医生。对这种复杂疾病及其多样表现有基本的了解对于预防严重危及生命的并发症至关重要。

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