Antithrombin Iii Deficiency
Mostrando 1-12 de 21 artigos, teses e dissertações.
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1. Manejo obstétrico de la deficiencia hereditaria de antitrombina durante el embarazo y puerperio. Dos casos clínicos
Abstract Introduction: hereditary antithrombin III deficiency is a rare disease that affects 0.02-0.2% of the population. It may be associated with a higher rate of complications and adverse outcomes in both mother and fetus. The present study describes the management of a woman with antithrombin III deficiency and two consecutive pregnancies. Description:
Rev. Bras. Saude Mater. Infant.. Publicado em: 2015-12
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2. Trombofilias maternas hereditárias com e sem tromboembolismo venoso: resultados maternos e neonatais / Maternal inherited thrombophilias with or without venous thromboembolism: maternal and neonatal outcomes
The aim of this study was to evaluate differences in maternal and neonatal outcomes in pregnancies complicated by inherited thrombophilias between patients with and without venous thromboembolism. Despite increasing evidence in the literature indicating an association between inherited thrombophilias and adverse obstetric outcomes, doubts remain whether thro
Publicado em: 2010
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3. Defeito bioquÃmico em fator V, fator V de Leiden, em paciente jovem com trombose venosa profunda: estudo de caso
Inherited disturbances of the coagulation and fibrinolysis have been associated with thrombophilia. Trauma can be a precipitant of the deep vein thrombosis (DVT) in Factor V Leiden (FVL) carriers, the most common polymorphism cause of hereditary thrombophilia. The objective of this study was to analyze the case of a 15 years old boy, his parents and a contro
Publicado em: 2001
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4. Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds.
Using DNA probes in a structural study of the antithrombin III gene locus we found no evidence of gene deletion in two British kindreds with inherited antithrombin III deficiency. However, linkage analysis between a common DNA polymorphism and the antithrombin III deficiency trait showed that the defect lies at or close to the antithrombin III structural gen
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5. Antithrombin III: summary of first database update.
Antithrombin III is the most important inhibitor of coagulation proteinases such as thrombin and factor Xa. Inherited deficiency of antithrombin III is a well recognised risk factor for the early development of venous thromboembolism. The gene for antithrombin III is located at chromosome 1q 23-25 and its structural organisation has been described. A databas
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6. Antithrombin-III deficiency in a Dutch family
A Dutch family (family A) with inherited antithrombin-III deficiency and an increased incidence of venous thrombosis was investigated. Antithrombin-III levels were measured by means of a coagulation assay in plasma and by single radial immunodiffusion in plasma and serum.
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7. Effect of danazol on the biochemical abnormality of inherited antithrombin III deficiency.
Seven members of a family affected by hereditary antithrombin III deficiency were identified. The disorder was associated with recurrent spontaneous episodes of phlebitis, deep venous thrombosis, and pulmonary embolism in middle age. Danazol, a 17-alkyl derivative of ethinyl testosterone, which has been used to treat other antiprotease deficiency states, was
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8. Antithrombin III deficiency and cerebrovascular accidents in young adults.
A young man with antithrombin III (AT-III) deficiency sustained a cerebellar venous infarct and recovered following treatment with AT-III concentrate. A family study showed that other members were affected. AT-III deficiency in this family was found to be due to a new variant AT-III TRURO 1. Young patients with strokes should be screened for thrombophilia.
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9. Overtight nappy precipitating thrombosis in antithrombin III deficiency.
An antithrombin III deficient infant presented with iliac vein thrombosis, apparently precipitated by an overtight nappy. Venous thrombosis is unusual, both in normal and in antithrombin III deficient children, but children with venous thrombosis should have their natural anticoagulants assayed and obvious risk factors avoided.
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10. Familial antithrombin III deficiency and Mycoplasma pneumoniae pneumonia.
A 10 year old girl presented with a massive femoral vein thrombosis associated with Mycoplasma pneumoniae pneumonia. Subsequently type I familial antithrombin III deficiency was diagnosed. It is suggested that prophylactic measures aimed at preventing thrombosis should be considered in acutely ill subjects with infection and familial thrombophilia.
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11. Acute Aortic Thrombosis and Antithrombin III Deficiency in the Nephrotic Syndrome: A Case Report
A 25-year-old Oriental woman with nephrotic syndrome was admitted to the United States Naval Hospital in Okinawa. She had acute aortic thrombosis, which was managed initially with bilateral femoral thrombectomy and calf fasciotomies. In the early postoperative period, increasing doses of heparin were required to maintain adequate anticoagulation. Hematologic
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12. Acquired antithrombin III deficiency and systemic lupus erythematosus.