نتایج جستجو برای: hereditary thrombophilia

تعداد نتایج: 87725  

Journal: :Srpski arhiv za celokupno lekarstvo 2010
Predrag Miljić Evelien Heylen Johan Willemse Valentina Djordjević Dragica Radojković Milica Colović Ivo Elezović Dirk Hendriks

Although the maintenance of precise balance between coagulation and fibrinolysis is of utmost importance for normal haemostasis, until recently these two systems were considered as completely separate mechanisms involved in the process of formation and dissolution of blood clot. Thrombin activatable fibrinolysis inhibitor (TAFI) is a recently described attenuator of the fibrinolytic rate and is...

Journal: :Blood 2012
Susanne Holzhauer Neil A Goldenberg Ralf Junker Christine Heller Monika Stoll Daniela Manner Rolf Mesters Anne Krümpel Michael Stach Ulrike Nowak-Göttl

Screening for inherited thrombophilia (IT) is controversial; persons at high risk for venous thromboembolism (VTE) who benefit from screening need to be identified. We tested 533 first- and second-degree relatives of 206 pediatric VTE patients for IT (antithrombin, protein C, protein S, factor V G1691A, factor II G20210A) and determined the incidence of symptomatic VTE relative to their IT stat...

Journal: :Ginekologia polska 2016
Oner Aynıoglu Hatice Isik Ahmet Sahbaz Husnu Alptekın Ulku Bayar

OBJECTIVES Recurrent pregnancy loss (RPL) is a serious problem in the reproductive age women. We aimed to study the role of anticoagulant therapy on pregnancy complications and perinatal outcomes in pregnant patients with histories of RPL. MATERIAL AND METHODS One hundred fifty-three pregnants, with RPL history and thrombophilia positivity, were grouped into two as 89 treated with anticoagula...

Journal: : 2022

Abstract Thrombophilia is a blood coagulation disorder, in which has an increased tendency to clot, with both arterial and venous localization, being responsible for multiple manifestations: secondary hypertension, stroke, acute pancreatitis or intracardiac masses. We are presenting the case of 21-year-old male patient, hypertensive, known thrombophilia, who was sent echocardiographic evaluatio...

2010
Theodore Emmanuelle Belkys Husein Javaid Iqbal M Macheta Peter Isaacs

INTRODUCTION Hereditary causes of visceral thrombosis or thrombosis should be sought among young patients. We present a case of a young man presenting with multiple hepatic infarctions resulting in portal hypertension due to homozygosity of the prothrombin gene mutation not previously described in literature. CASE PRESENTATION A 42-year-old Caucasian man with a previous history of idiopathic ...

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