Results 1 to 10 of about 2,368,168 (302)
R353Q polymorphism in the factor VII gene and cardiovascular risk in Heterozygous Familial Hypercholesterolemia: a case-control study [PDF]
Lipids in Health and Disease, 2011 Background Heterozygous Familial Hypercholesterolemia (FH) is a genetic disorder characterized by a high risk of cardiovascular disease. Certain polymorphisms of the factor VII gene have been associated with the development of coronary artery disease and
Pérez-Jiménez Francisco +9 more
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A 5-year-old Chinese boy with mild symptoms despite severe congenital factor VII deficiency: A case report [PDF]
Journal of International Medical ResearchCongenital factor VII deficiency is a rare autosomal recessive bleeding disorder characterized by markedly heterogeneous clinical phenotypes and reduced plasma factor VII activity.
Wei Luo +3 more
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Combined Factor VII and X Deficiency [PDF]
Online Journal of Health & Allied Sciences, 2011 Factor VII deficiency and factor X deficiency and very rare disorders individually. Combined Factor VII and X is a rare congenital blood disorder with very few cases reported in the literature.
Gursharan Singh Narang, +2 more
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A Neonate with Acquired Factor VII Deficiency Successfully Managed with Immunomodulatory Therapy
International Journal of Pediatrics & Adolescent Medicine, 2021 Acquired factor VII deficiency secondary to circulating inhibitors is rare in children but is a potentially life-threatening condition. Such a disease is challenging to diagnose and often difficult to manage.
Nof Saadi Alqarni, Ali H. Algiraigri
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Seminars in Thrombosis and Hemostasis, 2009 The complex formed between the procoagulant serine protease activated factor VII (FVII) and the membrane protein tissue factor, exposed on the vascular lumen upon injury, triggers the initiation of blood clotting. This review describes the clinical picture of FVII deficiency and provides information on diagnosis and management of the disease.
G. Mariani, BERNARDI, Francesco
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Polymorphisms in F2, F7, and PAI1 genes in men with coronary atherosclerosis
Российский кардиологический журнал, 2020 Aim. To study the associations of polymorphisms in F2, F7, and PAI1 genes with the presence of vulnerable plaque in coronary arteries (CA) and the blood concentration of proteins encoded by these genes.Material and methods.
E. V. Stryukova +7 more
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Thrombosis Journal, 2023 Background Factor VII deficiency is a rare bleeding disorder caused by a deficiency of clotting factor VII. However, there have been some case reports of venous thrombosis in patients with factor VII deficiency, especially underlying the prothrombotic ...
Lei Li +4 more
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Congenital Factor VII Deficiency Presenting with Isolated Recurrent Hematuria: A Case Report
Acta Medica Iranica, 2021 Introduction: Factor VII deficiency is a rare congenital coagulopathy disorder. In most cases this disorder is diagnosed in childhood. Common symptoms of congenital factor VII deficiency are different and consist of mucosal cutaneous hemorrhage ...
Shahla Ansary Damavandi +3 more
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Case Report: Factor VII Deficiency Presented With Cephalohematoma After Birth
Frontiers in Pediatrics, 2021 Introduction: Factor VII deficiency is a rare inherited autosomal recessive bleeding disorder with a global prevalence of 1/500,000. Most cases remain asymptomatic, and cases with severe clinical presentation are rarely reported.Case Presentation: A ...
Yuan-Chun Lo +3 more
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Blood Coagulation & Fibrinolysis, 2002 As yet, there have been neither systematic reviews nor reports of randomized, controlled trials involving factor VII (FVII) deficiency. Hence, a picture of this disorder can only be drawn by reviewing and summarizing the data that is available. This article provides an overview of the understanding of this rare, inherited disorder of coagulation.
openaire +3 more sources