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Treating a Patient of Dysfibrinogenemia with Acute Thromboembolism by Rivaroxaban and Cilostazol

Congenital dysfibrinogenemia is a rare autosomal recessive bleeding disorder, which is characterized by the absence of functional fibrinogen. Patients may have bleeding and paradoxical arterial and venous thrombotic problems from early childhood. The optimal antithrombotic therapy in these patients...

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Bibliografske podrobnosti
izdano v:Indian J Hematol Blood Transfus
Main Authors: Ozker, Emre, Atalay, Figen, Gulmez, Oyku, Saritas, Bulent
Format: Artigo
Jezik:Inglês
Izdano: Springer India 2016
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5544642/
https://ncbi.nlm.nih.gov/pubmed/28824252
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-016-0751-2
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