dc.creatorAndrade F.L.
dc.creatorAnnichino-Bizzacchi J.M.
dc.creatorSaad S.T.O.
dc.creatorCosta F.F.
dc.creatorArruda V.R.
dc.date1998
dc.date2015-06-30T15:05:32Z
dc.date2015-11-26T15:13:28Z
dc.date2015-06-30T15:05:32Z
dc.date2015-11-26T15:13:28Z
dc.date.accessioned2018-03-28T22:23:35Z
dc.date.available2018-03-28T22:23:35Z
dc.identifier
dc.identifierAmerican Journal Of Hematology. , v. 59, n. 1, p. 46 - 50, 1998.
dc.identifier3618609
dc.identifier10.1002/(SICI)1096-8652(199809)59:1<46::AID-AJH9>3.0.CO;2-#
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0031825212&partnerID=40&md5=b5c48463bd90a9b79bb93c3aaa8bc15e
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/100567
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/100567
dc.identifier2-s2.0-0031825212
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1258648
dc.descriptionThe prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homozygosity for transition 677C→T in the methylenetetrahydrofolate reductase (MTHFR) gene was determined among patients with sickle cell disease (SCD). The group included 73 patients with median age of 32,3 years with a diagnosis of sickle cell anemia in 53 patients, hemoglobinopathy SC in 16 patients, and four with S/β°thalassemia. Vascular complications such as ischemic stroke or deep vein thrombosis were diagnosed in nine patients. Heterozygosity for the prothrombin gene variant or factor V Leiden mutation was identified in four patients. However, only one patient, who developed ischemic stroke, was identified as a carrier of factor V Leiden mutation. None of the patients presented homozygosity for the thermolabile variant of the MTHFR. These data suggest a low clinical impact of inherited hypercoagulability risk factors in developing thrombosis, occlusive stroke, or mortality data among patients with SCD in Brazil.
dc.description59
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dc.description46
dc.description50
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dc.languageen
dc.publisher
dc.relationAmerican Journal of Hematology
dc.rightsfechado
dc.sourceScopus
dc.titleProthrombin Mutant, Factor V Leiden, And Thermolabile Variant Of Methylenetetrahidrofolate Reductase Among Patients With Sickle Cell Disease In Brazil
dc.typeArtículos de revistas


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