American Journal of Hematology · 2001 · 114 citations · 5 references
MedicineGeneticsHematologyHuman GeneticsIron Metabolism DisordersMedical GeneticsAnemiaHematologic DisordersIron DeficiencyIron Deficiency DisordersRed Blood Cell DisordersAnemia DiagnosisAnemia DiagnosticsDifferential Diagnosis CriteriaHemoglobin Levels
Red cell distribution width (RDW) was studied in adults carrying delta-beta thalassemia traits (deltabeta-TT) who were 20-40 years of age (n = 29), beta thalassemia traits (beta-TT) with an age range of 18-60 years (n = 49), iron deficiency anemia (IDA) in individuals aged 1-18 years (n = 27), and in controls with an age range of 20-40 years (n = 20). Although red blood cell count, MCV, and MCH values showed no statistically significant differences between deltabeta-TT and beta-TT, the mean RDW value was significantly higher in deltabeta-TT (20.14 +/- 1.21) compared to beta-TT (14.88 +/- 1.77) (P < 0.001). No difference was observed between the means of RDW in deltabeta-TT and IDA (18.00 +/- 1.94) (P > 0.05). A significant rise in RDW in IDA 5-7 days after initiation of iron therapy (P = 0.00) which was continued to rise up to the 4(th) week of therapy was suggested as an important tool in differentiation of IDA from deltabeta-TT. These observations could be kept in mind in the differential diagnosis of deltabeta-TT from beta-TT and IDA by determining the red blood cell count, red cell indices, and RDW only.
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Jorge Artaza, C D Carbia, M F Ceballo et al. · PubMed · 1999 · 51 citations
Medicine, Hematology, Pathology +17
Molecular analysis of the Turkish form of deletion‐inversion (δβ)° thalassaemia
H. Balkan, A. GU ̈RGEY, A. YALC ̧IN et al. · British Journal of Haematology · 1997 · 14 citations · Full text
A Novel (δβ)°-Thalassemia due to a ∼30-kb Deletion Observed in a Turkish Family
R. Öner, Çağrı Öner, Günhan Erdem et al. · Acta Haematologica · 2009 · 11 citations