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heterozygous factor v leiden mutation

Factor V Leiden Mutation and its Impact on Pregnancy Complications

Factor V Leiden Mutation and its Impact on Pregnancy Complications

... nancy outcomes such as placental abruption were rare. Eclampsia, intrauterine fetal death and venous thrombo- embolism did not occur. Thromboprophylaxis may have influenced the prevalence of VTE. The incidence of blood ...

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Impact of the factor V Leiden mutation on the outcome of pneumococcal pneumonia: a controlled laboratory study

Impact of the factor V Leiden mutation on the outcome of pneumococcal pneumonia: a controlled laboratory study

... FVL mutation impacts on local or systemic activation of coagulation in pneumo- coccal pneumonia we determined levels of TATc and FDP in lung homogenates (Figures 1a and 1b) and plasma (Figures 1c and 1d) in WT, ...

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Factor V Leiden, MTHFR C677T and Prothrombin Gene Mutation G20210A in Iranian Patients with Venous Thrombosis

Factor V Leiden, MTHFR C677T and Prothrombin Gene Mutation G20210A in Iranian Patients with Venous Thrombosis

... (C677T) mutation among our subjects was ...homozygous mutation was higher in ...the heterozygous state of the ...MTHFR mutation have a higher risk of thrombotic events during pregnancy such as ...

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Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease

Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease

... FVL mutation in the study population and its association with SCD is summarized in Table ...FVL mutation in its homozygous and heterozygous forms was found in 20 out of 117 patients for an overall ...

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FACTOR 5 LEIDEN STUDY OF GENETIC POLYMORPHISMS AS GENETIC FACTORS THAT CAUSE CARDIOVASCULAR DISEASE IN THE POPULATION OF TABRIZ, IRAN

FACTOR 5 LEIDEN STUDY OF GENETIC POLYMORPHISMS AS GENETIC FACTORS THAT CAUSE CARDIOVASCULAR DISEASE IN THE POPULATION OF TABRIZ, IRAN

... the factor V Leiden ...the mutation from a parent (heterozygous) increases by fourfold to eightfold the chance of developing a ...the mutation (homozygous), one from each parent, ...

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Myotonic Dystrophy-1 Complicated by Factor-V (Leiden) Mutation

Myotonic Dystrophy-1 Complicated by Factor-V (Leiden) Mutation

... a Leiden mutation, even if present in a heterozygous form, may severely affect DM1 patients to such a degree that they die from its long- term ...

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Maternal Factor V Leiden Mutation in Pre- eclampsia: A Case-Control South Eastern Indian Tertiary Care Hospital Based Study

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... the Leiden variant was ...The Leiden variant of factor V was not found in homozygous condition in either of the study ...the heterozygous condition is more in controls the FVLM was not ...

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Recurrent Pregnancy Loss in a Subject with Heterozygote Factor V Leiden Mutation; a Case Report

Recurrent Pregnancy Loss in a Subject with Heterozygote Factor V Leiden Mutation; a Case Report

... in Factor V Leiden heterozygotes and thrombotic risk is increased 10- to 80-fold in homozygotes (19- ...the factor V Leiden mutation in 22 of 110 women with obstetrical ...

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Relationship between  Methylenetetrahydrofolate Reductase (C677T), Factor V Leiden (G1691A),  Prothrombin Mutation (G20210A) and  Severe Preeclampsia in a Brazilian  Population

Relationship between Methylenetetrahydrofolate Reductase (C677T), Factor V Leiden (G1691A), Prothrombin Mutation (G20210A) and Severe Preeclampsia in a Brazilian Population

... FV Leiden and FII mutation carrier were ...were heterozygous and concomitance of both mutations was not ...FV Leiden, FII G20210A mutation and MTHFR C677T were not risks for ...

9

Lipoprotein (a): Its Role in Childhood Thromboembolism

Lipoprotein (a): Its Role in Childhood Thromboembolism

... the factor V Leiden mutation, 10 showed protein C deficiency, 2 showed antithrombin deficiency, and 4 showed primary antiphospholipid ...were heterozygous for the factor V ...

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Severe hyperhomocysteinemia due to cystathionine β-synthase deficiency, and Factor V Leiden mutation in a patient with recurrent venous thrombosis

Severe hyperhomocysteinemia due to cystathionine β-synthase deficiency, and Factor V Leiden mutation in a patient with recurrent venous thrombosis

... this subgroup the median age at diagnosis was 47 years (range 19-83), and the median level of tHcy was 130 μmol/L (range 101-262). Recurrent thrombosis occurred in 42% of cases [10]. In seven families in a consanguinous ...

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The relationship of the factor V Leiden mutation or the deletion deletion polymorphism of the angiotensin converting enzyme to postoperative thromboembolic events following total joint arthroplasty

The relationship of the factor V Leiden mutation or the deletion deletion polymorphism of the angiotensin converting enzyme to postoperative thromboembolic events following total joint arthroplasty

... of factor V resulting in resistance to the anticoagulant action of activated pro- tein C (APC) ...the Leiden Thrombophilia Study, which followed 474 consecutive patients of less than 70 years of age ...

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A case series of Factor V Leiden mutation in pregnancy

A case series of Factor V Leiden mutation in pregnancy

... FVL mutation and in particular patients with heterozygosity for the ...with heterozygous FVL mutation reported only a family history of VTED and 1 patient had a previous uncomplicated pregnancy for ...

5

Coagulopathy triggered autoimmunity: experimental antiphospholipid syndrome in factor V Leiden mice

Coagulopathy triggered autoimmunity: experimental antiphospholipid syndrome in factor V Leiden mice

... Figure 2 Effects of antiphospholipid syndrome (APS) induction on behavior and cognition in factor V Leiden (FVL) mice. (A) Cognitive function in a swim T-maze alternation test. The results are ...

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Relationship between angiotensin I-converting enzyme insertion/deletion gene polymorphism and retinal vein occlusion

Relationship between angiotensin I-converting enzyme insertion/deletion gene polymorphism and retinal vein occlusion

... resistance, factor V Leiden mutation, prothrombin 20210 mutation, mean platelet volume, homocysteine, PAI-1 and lipoprotein A ...

6

Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency

Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency

... Our fmdings clearly support the contention that the presence of simultaneous genetic defects increased the risk for thrombosis in anti- thrombin type I and II RS or PE: 92% of carriers o[r] ...

5

Factor V Leiden mutation triggering four major complications to standard dose cisplatin-chemotherapy for testicular seminoma: a case report

Factor V Leiden mutation triggering four major complications to standard dose cisplatin-chemotherapy for testicular seminoma: a case report

... With regard to the Bleomycin-related pulmonary fi- brosis the patient used to be a non-smoker and he had no apparent predisposing pulmonary conditions. Yet, two minor precipitating factors could be noted, i.e. the ...

5

High factor VIII levels contribute to the thrombotic risk in families with factor V Leiden

High factor VIII levels contribute to the thrombotic risk in families with factor V Leiden

... In order to explam the different venous thrombotic nsks in first-degree relatives of probands of selected thrombophilic families and first-degree relatives of unselected patients with th[r] ...

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Pulmonary Embolism in a Sarcoidosis Patient Double Heterozygous for Methylenetetrahydrofolate Reductase Gene Polymorphisms and Factor V Leiden and Homozygous for the D-Allele of Angiotensin Converting Enzyme Gene

Pulmonary Embolism in a Sarcoidosis Patient Double Heterozygous for Methylenetetrahydrofolate Reductase Gene Polymorphisms and Factor V Leiden and Homozygous for the D-Allele of Angiotensin Converting Enzyme Gene

... Rebeiz and colleagues [12] have described the first case in the literature of a young Lebanese man being diagnosed with sarcoidosis after presenting with pulmonary embolism, diffuse arterial thrombosis of the lower ...

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