Results 11 to 20 of about 7,596 (176)

The unexpected clot: unilateral brachial artery occlusion unmasking antithrombin III deficiency; case report and therapeutic considerations. [PDF]

Thromb J
Background Antithrombin III (AT III) deficiency is a rare autosomal dominant thrombophilia that typically predisposes carriers to venous thromboembolism.
Ishqair MA, Abu Jheasha AA, Ishqair AA, Khalili A, Isayed RMA, Zarari UAM.   +5 more
europepmc   +2 more sources

Antithrombin III deficiency and idiopathic intracranial hypertension: a case report. [PDF]

J Med Case Rep
Background Idiopathic intracranial hypertension (IIH) is a condition where the pressure of the cerebrospinal fluid in the brain increases without a known cause.
Togha M, Mokary Y, Jafari E.
europepmc   +2 more sources

Case report: A case of new mutation in SERPINC1 leading to thrombotic microangiopathy

Frontiers in Genetics, 2023
Introduction: Hereditary antithrombin-III deficiency can significantly increase the risk for thrombosis, which is common in limb deep vein and pulmonary cases. However, thrombotic microangiopathy (TMA) caused by hereditary antithrombin deficiency is rare.
Bing Li, Xiaohui Zhang, Hailin Lv, Xiaoqing Yang, Yanxia Gao, Zhao Hu, Chengjun Ma   +6 more
doaj   +1 more source

Management of antithrombin III deficiency in pregnancy: a representative case and a literature review

Акушерство, гинекология и репродукция, 2021
The work is aimed at discussing pregnancy management for the most thrombogenic genetic thrombophilia - antithrombin III (AT-III) deficiency. A detailed analysis of the literature and clinical case of pregnancy management in a patient with AT-III ...
S. V. Akinshina, P. K. Genina, V. O. Bitsadze, J. Kh. Khizroeva, V. I. Tsibizova, A. D. Makatsariya   +5 more
doaj   +1 more source

A Study of Prothrombotic Factors in Human Immunodeficiency Virus-Infected Patients

Indian Journal of Medical Specialities, 2021
Introduction: Human immunodeficiency virus (HIV) infection has been described as a hypercoagulable state. Some studies suggest that thrombotic events may be 2–10 times more prevalent in this group than in the general population.
Meena Lanjiwar, Pushpa Kumari, Jitendra Mohan Khunger, Narender Singh Negi   +3 more
doaj   +1 more source

Screening for inherited thrombophilias and prophylaxis of venous thromboembolism in pregnancy and puerperium [PDF]

Romanian Journal of Medical Practice, 2020
Thrombophilias are a group of coagulation disorders associated with a predisposition to thrombotic events. They could be inherited (genetic) or acquired. The most encountered inherited thrombophilias are factor V Leiden (FVL), prothrombin gene mutation (
Ana SCUTELNICU, Corina GICA, Radu BOTEZATU, Nicolae GICA, Anca Marina CIOBANU, Brindusa CIMPOCA, Gheorghe PELTECU, Anca Maria PANAITESCU   +7 more
doaj   +1 more source

Antithrombin III level in children with nephrotic syndrome, its correlation to thromboembolic complications, and serum albumin level

Saudi Journal of Kidney Diseases and Transplantation, 2021
Nephrotic syndrome (NS) is one of the most common pediatric diseases with many complications. Thromboembolic complication is the most serious complication.
Sherin Khamis Hussein, Ahmed Hafez Mohammed, Rehab Ahmed Mohammed, Hadeer Abdelghafar   +3 more
doaj   +1 more source

Treatment and secondary prophylaxis of venous thromboembolism with direct oral anticoagulants in patients with severe hereditary thrombophilia

Italian Journal of Medicine, 2021
Deficiency of protein C (PC), protein S (PS), antithrombin III (AT III), and homozygosity or combined heterozygosity for Factor V Leiden (FVL) and Factor II (FII) 20210A mutation represent severe hereditary thrombophilia (SHT) and are associated with a ...
Pasquale Madonna, Anna Guida, Maria Gabriella Coppola, Paolo Tirelli, Ernesto Grasso   +4 more
doaj   +1 more source

Antithrombin III: Plasma Activity and Reference Range Among Nigerian Blood Donors

Nigerian Postgraduate Medical Journal, 2015
Background: Diagnosis of antithrombin III (ATIII) deficiency as a common cause of thrombophilia is primarily based on the determination of antithrombin levels in plasma using a functional activity assay or an immunological assay, but local reference ...
Vincent Oluseye Osunkalu, Okezie Obasi Kanu, Felix Ngwuli   +2 more
doaj   +1 more source

Tromboembolias múltiplas associadas a défice de anti-trombina III.

Acta Médica Portuguesa, 1991
Congenital deficiency of antithrombin III is considered as one serious primary hypercoagulable state. The authors present a case of deficiency of antithrombin III in a 28 years old young male, with aortic valve disease and several thromboembolic events ...
C Catarino, P M Silva, J Quininha, J Serra, N da Silva, E Antunes, R Ferreira, M de Oliveira, R Gracias, A Prates   +9 more
doaj   +1 more source