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一名 BstUI 多态性 COL5A1 基因携带者的双侧连续股四头肌腱断裂。

Bilateral consecutive rupture of the quadriceps tendon in a man with BstUI polymorphism of the COL5A1 gene.

机构信息

Department of Orthopaedic and Trauma Surgery, Campus Bio-Medico University, Trigoria Rome, Italy.

出版信息

Knee Surg Sports Traumatol Arthrosc. 2010 Apr;18(4):514-8. doi: 10.1007/s00167-009-1002-y. Epub 2009 Dec 3.

Abstract

A genetic component has been implicated in tendinopathies involving tendon rupture. Type V collagen, a quantitatively minor fibrillar collagen which forms heterotypic fibrils with type I collagen, plays a role in the regulation of the size and configuration of fibrils of the much more abundant component type I collagen. To date, no data on the genetic component of bilateral rupture of the quadriceps tendon have been reported. We describe the presence of BstUI polymorphism of the COL5A1 gene in a man with bilateral rupture of the quadriceps tendon. The COL5A1 (the variant rs12722, BstUI RFLP) can be a candidate gene associated with the development of bilateral quadriceps tendon rupture.

摘要

遗传因素与涉及肌腱断裂的腱病有关。V 型胶原是一种定量上较少的纤维胶原,与 I 型胶原形成异质纤维,在调节更为丰富的 I 型胶原纤维的大小和结构方面发挥作用。迄今为止,尚无关于股四头肌腱双侧断裂遗传成分的报道。我们描述了一名双侧股四头肌腱断裂患者 COL5A1 基因 BstUI 多态性的存在。COL5A1(变体 rs12722,BstUI RFLP)可能是与双侧股四头肌腱断裂发展相关的候选基因。

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