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dc.creatorGuevara O,Carlos
dc.creatorNogales-Gaete,Jorge
dc.creatorFigueroa R,Tatiana
dc.creatorSáez M,David
dc.creatorValenzuela T,Daniel
dc.date2002-01-01
dc.date.accessioned2019-11-14T12:53:02Z
dc.date.available2019-11-14T12:53:02Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0034-98872002000100011
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/115752
dc.descriptionHereditary hypercoagulability has been identified as risk factor in approximately 30% of cerebral venous thrombosis cases. We report three females with this association. A 38 years old female with a history of deep venous thrombosis of the lower limb, presented with headache, vomiting and a generalized seizure. Magnetic resonance angiography showed a partial thrombosis of the left lateral and superior longitudinal venous sinuses. Coagulation study showed a resistance to activated C protein and factor V Leyden. A 42 years old woman with a history of deep venous thrombosis, presented a right hemiplegia during a hospitalization. Magnetic resonance showed a left lateral hemorrhagic infarction. Magnetic resonance angiography showed an absence of signal in three venous sinuses. Coagulation study showed a protein C deficiency. A 17 years old woman presented a right hemiparesis in the sixth day of puerperium. CAT scan showed a left frontoparietal subcortical venous infarction. Coagulation study showed an antithrombin III deficiency (Rev Méd Chile 2002; 130: 79-85)
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dc.publisherSociedad Médica de Santiago
dc.relation10.4067/S0034-98872002000100011
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceRevista médica de Chile v.130 n.1 2002
dc.subjectAntithrombin III deficiency
dc.subjectProtein C deficiency
dc.subjectThrombofilia
dc.subjectThrombosis
dc.titleEstados de hipercoagulabilidad heredados y trombosis venosa cerebral: Experiencia en 3 casos


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