American Journal of Hematology · 2008 · 146 citations · 9 references
MedicineHematologyClinical Classification SystemsMedical GeneticsTransfusion MedicineAnemiaClinical HematologyHematologic DisordersRed Blood Cell DisordersSickle Cell DiseaseAnemia ClassificationClinical HeterogeneityDisease Severity EstimationGenotype-phenotype AssociationsHemoglobin LevelsHeterogeneityPhenotypic Diversity AnalysisSpleen Size
Beta-thalassemia intermediate patients show a remarkable clinical heterogeneity. We examined the phenotypic diversity of 950 beta-thalassemia/Hb E patients in an attempt to construct a system for classifying disease severity. A novel scoring system based on six independent parameters, hemoglobin level, age at disease presentation, age at receiving first blood transfusion, requirement for transfusion, spleen size, and growth and development, was able to separate patients into three distinctive severity categories: mild, moderate, and severe courses. This system, therefore, can increase the accuracy of studies of genotype-phenotype interactions and facilitate decisions for appropriate patient management.
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Genetic modifiers of beta-thalassemia.
Swee Lay Thein · PubMed · 2005 · 191 citations
Life Sciences, Genetics, Hematology +11
Haemoglobin E β thalassaemia in Sri Lanka
Anuja Premawardhena, CA Fisher, NF Olivieri et al. · The Lancet · 2005 · 104 citations