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二尖瓣脱垂患者的关节过度活动。

Joint hypermobility in patients with mitral valve prolapse.

机构信息

Faculdade de Medicina de São José do Rio Preto, Rua Paraná 66, São José do Rio Preto, SP, Brazil.

出版信息

Arq Bras Cardiol. 2009 Sep;93(3):307-11. doi: 10.1590/s0066-782x2009000900016.

DOI:10.1590/s0066-782x2009000900016
PMID:19851660
Abstract

Studies on hypermobility have aroused great interest in the last decades, as they are associated to musculoskeletal disorders, as well as abnormalities in several organic systems, such as the mitral valve prolapse. Therefore, in this study, data on the association between joint hypermobility and the mitral valve prolapse were investigated and reviewed. Studies in the literature have shown that genetic alterations in the collagen composition seem to be the main cause of this association.

摘要

过去几十年的研究表明,关节过度活动与肌肉骨骼疾病以及多个器官系统的异常有关,如二尖瓣脱垂。因此,本研究调查并回顾了关节过度活动与二尖瓣脱垂之间的关系。文献中的研究表明,胶原成分的遗传改变似乎是这种关联的主要原因。

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1
Joint hypermobility in patients with mitral valve prolapse.二尖瓣脱垂患者的关节过度活动。
Arq Bras Cardiol. 2009 Sep;93(3):307-11. doi: 10.1590/s0066-782x2009000900016.
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Increased prevalence of mitral valve prolapse associated with an elevated skin type III/III+I collagen ratio in joint hypermobility syndrome.二尖瓣脱垂患病率增加与关节过度活动综合征中皮肤III型/III + I型胶原蛋白比例升高相关。
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Joint hypermobility syndrome and mitral valve prolapse in panic disorder.惊恐障碍中的关节过度活动综合征和二尖瓣脱垂
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Joint hypermobility syndrome: inherited disorder of collagen synthesis.关节过度活动综合征:胶原蛋白合成的遗传性疾病。
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A hypermobility study in ballet dancers.芭蕾舞演员的关节过度活动研究。
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Joint hypermobility in primary mitral valve prolapse patients.原发性二尖瓣脱垂患者的关节过度活动
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Genetic evidence that mutations in the COL1A1, COL1A2, COL3A1, or COL5A2 collagen genes are not responsible for mitral valve prolapse.有基因证据表明,COL1A1、COL1A2、COL3A1或COL5A2胶原蛋白基因的突变与二尖瓣脱垂无关。
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