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Article

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia.

Clinical chemistry and laboratory medicine - 1 Aug 2013

Sahli Chaima A, Bibi Amina, Ouali Faida, Fredj Sondess Hadj, Dakhlaoui Boutheina, Othmani Rym, Laaouini Naouel, Jouini Latifa, Ouenniche Fekria, Siala Hajer, Touhami Imed, Becher Mariem, Fattoum Slaheddine, El Houda Toumi Nour, Messaoud Taieb

Abstract excerpt

BACKGROUND: In Tunisia, thalassemia and sickle cell disease (SS) represent the most prevalent monogenic hemoglobin disorders with 2.21% and 1.89% of carriers, respectively. This study aims to evaluate the diagnosis reliability of 12 red blood cell (RBC) indices in differentiation of β-thalassemia trait (β-TT) from iron deficiency anemia (IDA) and between homozygous SS and sickle cell thalassemia (ST). METHODS:...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 23492565
DOI: 10.1515/cclm-2012-0842

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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