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首页> 外文期刊>Haemophilia: the official journal of the World Federation of Hemophilia >An update on the new classification of Ehlers-Danlos syndrome and review of the causes of bleeding in this population
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An update on the new classification of Ehlers-Danlos syndrome and review of the causes of bleeding in this population

机译:关于ehlers-danlos综合征的新分类的更新,并审查了这群人群中出血的原因

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It has long been hypothesized that bleeding symptoms in people with hypermobility occur as a result of abnormalities in the collagen of the vessel wall or the connective tissues. The bleeding symptoms, particularly in the skin, have been attributed to the fragility of skin and blood vessels caused by "defective collagen wickerwork" of the reticular layer of the skin. Collagen, which forms the framework of vessel walls, is altered in many patients with Ehlers-Danlos syndrome (EDS) leading to weakening of the vessel wall or the supporting tissues. Another important function of subendothe-lial collagen is its interaction with platelets and von Willebrand factor, which results in the propagation of a platelet plug. Thus, abnormalities in subendothelial collagen may alter its interaction with platelets and VWF. More recently, hypermobile-EDS (hEDS) has been associated with mast cell disorders, a condition independently associated with bleeding symptoms. It has also been observed that patients with mild bleeding disorders have a more severe bleeding phenotype when they have co-existing joint hypermobility.
机译:它已经假设是由于血管壁的胶原蛋白或结缔组织的异常发生了具有高兴的人们的出血症状。出血症状,特别是在皮肤上,归因于皮肤周围的“有缺陷的胶原柳制品”引起的皮肤和血管的脆弱性。形成血管壁框架的胶原蛋白在许多患有ehlers-danlos综合征(EDS)的患者中被改变,导致血管壁或支撑组织的弱化。潜水生子胶原蛋白的另一个重要功能是其与血小板和von Willebrand系数的相互作用,这导致血小板塞的传播。因此,潜水前胶原的异常可以改变其与血小板和VWF的相互作用。最近,Hypermobile-EDS(HEDS)与肥大细胞紊乱有关,其与出血​​症状独立相关的病症。还观察到,当它们具有共存关节性时,患有轻度渗出障碍的患者具有更严重的出血表型。

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