Antiphospholipid syndrome with hemophilia B: A case report represented by recurrent thrombosis/ bleeding attacks | Yokus | Pakistan Journal of Medical Sciences
 
مبل راحتی صندلی مدیریتی صندلی اداری میز اداری وبلاگدهی گن لاغری بازی اندروید تبلیغات کلیکی آموزش زبان انگلیسی پاراگلایدر مارکت اندروید تور آهنگ محسن چاوشی مسیح و آرش پروتز سینه پروتز باسن پروتز لب میز تلویزیون

Antiphospholipid syndrome with hemophilia B: A case report represented by recurrent thrombosis/ bleeding attacks

Osman Yokus, Yesim Uckurt, Ali Soner Demir, Semih Kalyon, Ozlem Sahin Balcik, Derya Akdeniz

Abstract


Antiphospholipid syndrome is a disease presenting with arterial/ venous thrombosis and obstetrical complications. Pulmonary embolism is an important pulmonary complication of antiphospholipid syndrome, whereas, intra-alveolar hemorrhage is a rarely encountered manifestation. Hemophilia B is caused by factor IX deficiency that results in prolonged oozing after injuries and/or surgery, and delayed or recurrent bleeding prior to complete wound healing. Antithrombotic therapy may be used for recurrent hemostatic attacks in APS; but if there is a hemostatic defect, it may lead to serious bleeding complications. Here, we present a case of antiphospholipid syndrome accompanied by heterozygote methylene tetrahydrofolate reductase gene mutation (MTHFR) mutation and hemophilia B.

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