Overview
Coagulation factor deficiencies are disorders in which the absence, reduced level, or impaired function of one or more clotting factors compromises the body's ability to form a stable fibrin clot, producing a bleeding tendency that ranges from mild to life-threatening. The coagulation cascade depends on the sequential activation of plasma proteins, and deficiency of any component disrupts thrombin generation and clot stabilisation. Inherited forms include haemophilia A and B, caused by deficiency of factors VIII and IX respectively and typically X-linked, and rarer autosomal disorders such as factor XI deficiency, also known as Rosenthal's disease or haemophilia C, which may present with mucosal bleeding such as chronic epistaxis. Deficiencies also arise from mutations affecting other coagulation factors and their regulatory proteins, underscoring the genetic heterogeneity of inherited bleeding disorders. Acquired deficiencies develop through autoantibody formation, as in acquired haemophilia, or secondary to liver disease, vitamin K deficiency, consumptive coagulopathy, and disturbances of von Willebrand factor and ADAMTS13 seen in haematological malignancy. Diagnosis combines clotting assays, factor-specific quantification, and inhibitor testing, while management uses factor replacement, bypassing agents, antifibrinolytics, and treatment of underlying causes. Research in this area characterises the molecular basis of factor defects, their clinical phenotypes, and improved strategies for prevention and control of bleeding.
Research published in this journal
6 peer-reviewed articles, ranked by relevance. Each links to its DOI.
Study of Hypercoagulability in Patients with Acute Leukaemia in the Hematology Department of Teaching Hospital of Yopougon (Abidjan)
Acquired Haemophilia: A Case Report and Literature Review
Haematological Disturbances in Dengue Haemorrhagic Fever - its Pathogenesis and Management Perspectives
Acquired Abnormalities of Plasma Von Willebrand Factor Related Parameters and ADAMTS13 Autoantibodies in Aggressive Haematological Malignancies.
Rosenthal's Disease (Hemophilia C or factor XI Deficiency) Revealed by Chronic Epistaxis: The First Observation in Sub-Saharan Africa.
How this research is being cited
The 6 articles above have been cited 17 times in the scholarly literature. Citation data via OpenAlex and Crossref, updated Jun 2026.
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Dina Ashraf Abdelhady et al. · 2025 · European Journal of Medical Research
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2025 · European journal of medical research
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2025 · Food and Agricultural Immunology
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Claudia Reytor-González et al. · 2025 · Food and Agricultural Immunology
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Archana Sreedharan et al. · 2024 · Journal of Ayurveda and Integrative Medicine
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Yogeshwar Parmanand Kapgate et al. · 2024 · Journal of Pharmacognosy and Phytochemistry
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2024 · Journal of Ayurveda and Integrative Medicine
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A. Begum et al. · 2023 · Bangladesh Critical Care Journal
A sample of recent works citing this journal's research on Coagulation Factor Deficiencies, linking to each citing work.