Celletti C, Camerota F
Physical Medicine and Rehabilitation Division, Orthopedic Department, Umberto I Hospital, Sapienza University, Rome, Italy.
Clin Ter. 2013;164(4):e325-35. doi: 10.7417/CT.2013.1597.
Joint hypermobility syndrome (JHS) is a hereditary disorder of connective tissue recently considered the one and the same as the Ehlers-Danlos Syndrome Hypermobility Type (EDS-HT). The JHS/EDS-HT is mainly characterized by joint hypermobility, chronic pain and a variable skin involvement. Clinical manifestations expressed by patients are multiple and varied. The rehabilitative approach may play a fundamental role in the understanding and management of symptoms and clinical manifestation. Aim of this study is to make a literature revision of all the aspects of this not so rare disease.
关节过度活动综合征(JHS)是一种结缔组织遗传性疾病,最近被认为与埃勒斯-当洛综合征过度活动型(EDS-HT)是同一种疾病。JHS/EDS-HT的主要特征是关节过度活动、慢性疼痛和不同程度的皮肤受累。患者表现出的临床表现多种多样。康复方法可能在症状和临床表现的理解及管理中发挥重要作用。本研究的目的是对这种并不罕见的疾病的各个方面进行文献综述。