Article
Prothrombin G20210A and methylenetetrahydrofolate reductase C677T polymorphisms in peripheral capillary nonperfusion: a case report.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Sept 2015
Wathek Chaima, Mrad Meriem, Abdessalem Nadia Ben, Maalej Afef, Gritli Nasreddine, Gabsi Salem, Rannen Riadh, Fekih-Mrissa Najiba
Abstract excerpt
The G20210A mutation in the prothrombin gene is an established risk factor for venous thrombosis. However, there is some controversy as to the role played by this mutation in arterial thrombotic disease. The association of peripheral capillary nonperfusion with prothrombin G20210A mutation has never been reported before. We present the case of 34-year-old man who presented with peripheral capillary nonperfusion....
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.