Inherited and acquired thrombophilia as a modifier of clinical course of chronic immune thrombocytopenia

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Inherited and Acquired Thrombophilia in Pregnancy

The thrombophilia represent a spectrum of coagulation disorders associated with a predisposition for thrombotic events (deep vein thrombosis (DVT) and pulmonary embolism (PE)) (Kaandorp et al, 2009). Inherited thrombophilia include a single-point mutation on the Factor V gene (factor V Leiden (FVL), prothrombin (PT) G20210A gene mutation, deficiencies in protein C and protein S as well as antit...

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CLINICAL TRIALS AND OBSERVATIONS Impact of immune thrombocytopenia on the clinical course of chronic lymphocytic leukemia

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Inherited Genetic Markers for Thrombophilia in Northeastern Iran (a Clinical-Based Report)

Background: Thrombophilia is a main predisposition to thrombosis due to a procoagulant state. Several point mutations play key roles in blood-clotting disorders, which are grouped under the term thrombophilia. These thrombophilic mutations are methylenetetrahydrofolate reductase (MTHFR, C677T, and A1298C), factor V Leiden (G1691A), prothrombin gene mutation (factor II, G20210A), and plasminogen...

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Inherited thrombophilia: pathogenesis, clinical syndromes, and management.

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Pregnancy and Issues with Inherited and Acquired Thrombophilia

Pregnancy is hypercoagulable state. The field of thrombophilia; the tendency to thrombosis, has been developed rapidly and has been linked to many aspects of pregnancy. It is recently that severe pregnancy complications such as severe preeclampsia, intrauterine growth retardation, abruptio placentae and stillbirth has been shown to be associated with thrombophilia. Recurrent miscarriage has als...

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ژورنال

عنوان ژورنال: Journal of Applied Hematology

سال: 2020

ISSN: 1658-5127

DOI: 10.4103/joah.joah_75_19