Overview
Blood coagulation disorders are conditions in which the haemostatic system fails to maintain the balance between clot formation and clot breakdown, producing either a tendency to abnormal bleeding or to pathological thrombosis. Normal haemostasis depends on the coordinated action of platelets, the coagulation factor cascade, von Willebrand factor, and natural anticoagulant and fibrinolytic pathways; disruption at any point disturbs this equilibrium. Bleeding disorders may be inherited, arising from genetic mutations in coagulation factors and their regulatory proteins, as in the haemophilias and rarer deficiencies such as factor XI deficiency, or acquired, including abnormalities of von Willebrand factor and ADAMTS13 that accompany malignancy. Classification distinguishes defects of primary haemostasis involving platelets and von Willebrand factor from defects of secondary haemostasis involving the coagulation factors, and separates congenital from acquired causes. Hypercoagulable states, by contrast, predispose to venous and arterial thrombosis and arise in settings such as acute leukaemia and other systemic illnesses, while infections and organ disease can perturb coagulation through consumption, dysregulation, or altered factor synthesis. Diagnosis relies on coagulation assays, factor measurement, and molecular and immunological testing. The study of these disorders links haematology, molecular genetics, and clinical medicine to clarify mechanisms of bleeding and thrombosis and to guide diagnosis, monitoring, and targeted treatment.
Research published in this journal
6 peer-reviewed articles, ranked by relevance. Each links to its DOI.
Acquired Abnormalities of Plasma Von Willebrand Factor Related Parameters and ADAMTS13 Autoantibodies in Aggressive Haematological Malignancies.
Haematological Disturbances in Dengue Haemorrhagic Fever - its Pathogenesis and Management Perspectives
Study of Hypercoagulability in Patients with Acute Leukaemia in the Hematology Department of Teaching Hospital of Yopougon (Abidjan)
Rosenthal's Disease (Hemophilia C or factor XI Deficiency) Revealed by Chronic Epistaxis: The First Observation in Sub-Saharan Africa.
Role of Tie2, CD14, Angiopoietin as Angiogenetic Markers in Hepatocellular Carcinoma Complicating Hepatitis C Virus Infection
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 Blood Coagulation Disorders, linking to each citing work.