ENFERMEDAD DE PERTHES PEDIATRIA PDF
A síndrome de Legg-Calvé-Perthes ou doença de Perthes é uma doença degenerativa da articulação da anca (quadril em português brasileiro) em que ocorre. El absceso del psoas es una enfermedad infrecuente en niños. Puede tener una en pediatría es primario; sin embargo, en ocasiones, puede ser de origen secundario y médula espinal, enfermedad de. Legg-Calvé-Perthes, entre otros Download Citation on ResearchGate | Enfermedad de Legg Calvé Perthes (LCP) en varios aspectos de la enfermedad de Legg Calvé Perthes y la evolución de caderas de August · Anales espanoles de pediatria.
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Background It has been suggested that the cause of Perthes diseasemay be intravascular thrombosis induced by a potentialcongenital hemostatic disorder leading to conditions ofthrombophilia or hyperfibrinolysis.
Alterations in hemostasis and thrombosis were detectedin one patient who had moderate-to-light protein Sdeficiency.
Thromb Haemost, 71pp. Clin Othop,pp. J Biol Chem,pp. Mutation in blood coagulation factor V associated with resistance to activated protein C. Anal Biochem,pp.
Relation of altered hemostasis to etiology. Are you a health professional able to prescribe or dispense drugs?
Síndrome de Legg-Calvé-Perthes
Determination of plasminogen activator and its fast inhibitor in plasma. Decreased fibrynolitic pertehs in patients with idio-pathic avascular necrosis and transient osteoporosis of the hip.
Familial hypofibrinolysis and venous thrombosis. Protein C and S deficiency, thrombofilia and hypofibrinolysis: Thromb Haemost, 62pp. Mutation in gene coding for factor V and the risk of myocardial infarction, stroke and venous thrombosis in apparently healthy men.
Blood, 82pp. Maturation of the hemostatic system during childhood. J Clin Invest, 94pp. Antithrombin heparin cofactor assay with new chromogenic substrates.
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J Lab Clin Med,pp. Am J Hematol, 45pp. The remaining patients were considered withinthe normal range when age was taken into account. The remaining patients were considered withinthe normal range when age was taken into account. It has been suggested that the cause of Perthes diseasemay be intravascular pediatroa induced by a potentialcongenital hemostatic disorder leading to conditions ofthrombophilia enrermedad hyperfibrinolysis. Conclusions Epidemiological and laboratory data from this group ofpediatric patients and from the control group do not supportthe hypothesis that a thrombogenesis defect couldbe the underlying cause of avascular necrosis of the hipjoint.
N Engl J Med,pp. Clin Orthop,pp. Association of idiopathic venous thromboembolism with single point-mutation at Arg of factor. Severe thrombotic disease in a young man with bone marrow and skeletal changes and with a high content of an inhibitor in the fibrinolytic system. Am J Hematol, 44pp. Variability of thrombosis among homozigous siblings with resistance to activated protein C due to an Arg-Gln mutaion in gen for factor V.
High risk of thrombosis in patients homozigous for factor V Leiden activated protein C resistance. Idiopathic osteonecrosis, hypofibrinolysis, high plasminogen activator inhibitor, high Lp aand therapy with stanozolol.
Enfermedad de Legg-Calve-Perthes | HCA Healthcare
Thromb Res, 11pp. Identification of the same factor V gene mutation in 47 of 50 thrombosis-prone families with inherited resistance to activated protein C.
Necesidades del alumnado con diabetes tipo 1 en Espectrophotometric solid-phase tissue plasminogen activator activity assay Sofia-tPA for high-fibrin-affinity tissue plasminogen activators.
Resistance to activated protein C and Legg-Perthes disease. Thromb Haemost, 69pp. Genetics aspects of Perthes disease: Special laboratory evaluation of coagulation.
J Med,pp. Blood, 85pp. The second international anticardiolipin standardization workshop. Pediatr Res, 35pp. Am J Clin Pathol, 94pp. Br J Enfermerad, 71pp. Epidemiological and laboratory data from this group ofpediatric patients and from the control group do not supportthe hypothesis that a thrombogenesis defect couldbe the underlying cause of avascular necrosis of the hipjoint.