Results 11 to 20 of about 14,445,357 (297)
Pakistan Armed Forces Medical Journal, 2022 Objective: To determine the diagnostic accuracy of clotting based APCR assay in determining Factor V Leiden mutation with PCR as gold standard and to establish the frequency of factor V Leiden mutation in patients presenting with thrombophilia as well ...
Sidra Barlas +5 more
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Radiologic technology, 2020 Factor V Leiden thrombophilia is a genetic mutation that results in hypercoagulation of the blood that presents life-threatening symptoms. This article describes the role of imaging in diagnosis and treatment of cardiovascular complications caused by factor V Leiden and summarizes the etiology, risk factors, symptoms, diagnostic measures, progression ...
Jason S, Applegate, Diane, Gronefeld
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A Rare Case of Quadruple Limb Amputation due to Factor V Leiden Mutation
Indian Journal of Physical Medicine & Rehabilitation, 2022 Factor V Leiden, an autosomal dominant gene mutation that leads to increase risk of forming thrombophilia. Amputation in patients with Factor V leiden mutation is known but none describe quad-limb amputation in this setting.
Ann Noble Zachariah, Ravi Sankaran
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Factor V Leiden and Inflammation [PDF]
Thrombosis, 2012 Factor V Leiden, is a variant of human factor V (FV), also known as proaccelerin, which leads to a hypercoagulable state. Along these years, factor V Leiden (FVL) has been studied from the pathophysiologic point of view, and research has been focused on finding clinical approaches for the management of the FVL associated to a trombophilic state.
Silvia Perez-Pujol +2 more
openaire +2 more sources
The Journal of Perinatal & Neonatal Nursing, 2003 Factor V Leiden, formed by a genetic mutation, disrupts the body's anticoagulation defense system. It was isolated as recently as 1994 as a risk factor for venous thromboembolism. Factor V Leiden has also been linked to preeclampsia, pregnancy loss, and fetal growth restriction.
Deborah L. Ornstein, Mary Cushman
openaire +3 more sources
Factor V Leiden and Prothrombin Mutations in South of Iran
Armaghane Danesh Bimonthly Journal, 2007 : Introduction & Objective: Factor V Leiden and prothrombin mutation are not common but they are involved in pediatric thrombosis. The aim of this study was to evaluate the frequency of factor V Leiden & prohtrombin mutation in healthy population of ...
M Karimi, AR Panahande, AR Afrasiabi
doaj +1 more source
Prevalence of the factor V Leiden mutation in patients susceptible to venous thromboembolism [PDF]
, 2020 Background. A tendency to venous thromboembolism is otherwise called hypercoagulability or thrombophilia. This disease can be acquired or have a genetic background, and may lead to pulmonary embolism. The basis for analysis and selection of treatment is
Elżbieta Wierszyło +6 more
core +1 more source
Mechanisms of the Factor V Leiden Paradox [PDF]
Arteriosclerosis, Thrombosis, and Vascular Biology, 2008 Objective— Carriers of the factor V Leiden mutation (FVL-carriers) have a substantially increased risk of deep venous thrombosis (DVT), whereas the risk of pulmonary embolism (PE) is only mildly increased compared with noncarriers.
van Stralen, K. J. +5 more
openaire +4 more sources
Indian Journal of Pathology and Microbiology, 2020 Background: Thrombophilia is a hypercoagulable state characterized by increased venous thrombosis. The most common cause of heritable thrombophilia is Factor V Leiden (FVR506Q) homozygous state, with a relative risk of 10–80 times as compared to normal ...
Mirza Asif Baig
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Maternal Factor V Leiden Mutation in Preeclampsia: A Case-Control South Eastern Indian Tertiary Care Hospital Based Study [PDF]
Journal of Clinical and Diagnostic Research, 2020 Introduction: Pre-Eclampsia (PE) is a pregnancy-specific disorder which further complicates and leads to eclampsia. The Factor V Leiden (FVL) is an autosomal dominant genetic abnormality with incomplete penetrance predisposes to thrombosis.
Krishnaveni Changalvala +6 more
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