Pediatric Hematology and Oncology · 1999 · 17 citations · 10 references
MedicineHematologyMolecular GeneticsHematopathologyHemostasisMedical GeneticsAnemiaDeep Vein ThrombosisSickle Cell DiseaseThromboembolic DiseaseThrombosisVenous ThromboembolismActivated Protein C ResistanceFactor V Leiden ThrombophiliaFactor V MutationMethylenetetrahydrofolate DehydrogenaseRecurrent Venous ThromboembolismSickle Cell AnemiaSickle Cell Disease-associated ThrombosisSickle Cell Disease-related Stroke
Vaso-occlusive crisis is the most common cause of morbidity in patients with sickle cell anemia (SCA). Central nervous system involvement that leads to hemiplegia is the most frequent neurological complication in those patients. Peripheral deep venous thromboembolism was not reported in SCA patients. Activated protein C resistance is associated with an increased risk of thrombophilia. The authors report an SCA patient with recurrent cerebrovascular accident and deep venous thrombosis. Activated protein C resistance due to factor V Leiden heterozygous and heterozygocity for the methylenetetrahydrofolate reductase were diagnosed and suspected to be the risk factors that contribute to the development of the deep vein thrombosis in this SCA patient.
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Björn Dahlbäck, Martin Carlsson, Peter J. Svensson · Proceedings of the National Academy of Sciences · 1993 · 2K citations
Ted Koster, FR Rosendaal, Hans de Ronde et al. · The Lancet · 1993 · 1.3K citations
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Paul M. Ridker, Charles H. Hennekens, Klaus Lindpaintner et al. · New England Journal of Medicine · 1995 · 1.1K citations · Full text
Abnormal Adherence of Sickle Erythrocytes to Cultured Vascular Endothelium
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Medicine, Cell Biology, Hematology +15
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Medicine, Genetics, Hematology +17