Recurrent pregnancy loss: can factor V Leiden mutations be a cause [PDF]
Obstetrics & Gynecology Science, 2019 The role of Factor V Leiden (FVL) mutation in recurrent miscarriages has been disputed. It has been hypothesized that FVL mutation in patients with recurrent miscarriages is treatable.
R R N Reddy +3 more
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Factor V Leiden Mutation in Iraqi Patients with Deep Venous Thrombosis.
مجلة كلية الطب, 2011 Background: Factor V Leiden is considered the most common inherited risk factor for venous thrombosis in Caucasian populations, including those in the Eastern Mediterranean region.
Nasir Al-Allawi +2 more
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Is Factor V Leiden a Risk Factor for Fetal Loss?
Acta Medica, 1999 A successful pregnancy is dependent on the development of adequate placental circulation. The abnormalities of placental vasculature may result in a number of gestational pathologies, including fetal loss.
Petr Dulíček +5 more
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Factor V Leiden thrombophilia [PDF]
Genetics in Medicine, 2011 Factor V Leiden is a genetic disorder characterized by a poor anticoagulant response to activated Protein C and an increased risk for venous thromboembolism. Deep venous thrombosis and pulmonary embolism are the most common manifestations, but thrombosis in unusual locations also occurs.
openaire +2 more sources
Revista Brasileira de Hematologia e Hemoterapia, 2006 As tromboses são eventos de etiopatogênese multifatorial resultantes da interação de fatores genéticos e ambientais, constituindo na atualidade uma das causas mais comuns de morbimortalidade.
Catarina P. S. Ramos +6 more
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Factor V Leiden mutation and pregnancy. Haemostasis during pregnancy in non-carriers and carriers of factor V Leiden mutation, with special emphasis on placenta-mediated and venous thromboembolic complications and on blood coagulation and fibrinolysis markers for prediction of complications [PDF]
, 2009 Factor V Leiden (FVL) mutation elevates the risk of venous thromboembolism (VTE) in general. During pregnancy, the haemostatic balance is changed in the direction of hypercoagulability, resulting in an increased incidence of VTE. 42 women were followed
Kjellberg, Ulla
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Современная ревматология, 2021 The article provides a description of the systemic lupus erythematosus patient with multiple avascular bone necrosis (ABN), homozygous mutation in clotting factor V (Leiden) gene, who successfully underwent the total hip replacement.
F. A. Cheldieva +4 more
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Factor V Leiden Mutation - an Unusual Cause of Hypopituitarism?
Endocrinology Research and Practice, 2022 Hypopituitarism is a disorder of diverse etiology that results in partial or total loss of pituitary functions. Here we report a 49-year-old female patient presenting with absence of peripheral pulses of the right upper extremity and anterior pituitary ...
Ekrem Algün +9 more
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Factor V Leiden and venous thrombosis: First case report from Iraq
مجلة كلية الطب, 2005 Background: Factor V Leiden mutation is the most common cause of hereditary thrombophilia . this mutation was found to be highly prevalent in the Eastern Mediterranean region , with recently reported prevalence of 3% in random Iraqi blood donors.
Nasir AL-Allawi +3 more
doaj +1 more source
Evaluation of Genetic and Environmental Risk Factors for Deep Vein Thrombosis in Sudanese [PDF]
Journal of Clinical and Diagnostic Research, 2018 Introduction: Thrombophilia is a multi-factorial hypercoagulability disorder. The predisposing factors may be inherited, acquired or both. Factor V Leiden prothrombin 20210G>A mutations are the most common inherited factors.
Nadir Ahmed Ibrahim +3 more
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