δβ-Thalassemia Trait | Zendy

Diego VelascoRodríguez | Zendy; Juan Manuel AlonsoDomínguez | Zendy; Fernando-Ataúlfo González-Fernández | Zendy; Jesús Villarrubia | Zendy; Paloma Ropero | Zendy; Jorge Martínez Nieto | Zendy; Félix de la Fuente | Zendy; Raquel Guillén | Zendy; Natalia Acedo | Zendy; Cristina Serí | Zendy; Fernando Cava | Zendy

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δβ-Thalassemia Trait

Author(s) -

Diego VelascoRodríguez,

Juan Manuel AlonsoDomínguez,

Fernando-Ataúlfo González-Fernández,

Jesús Villarrubia,

Paloma Ropero,

Jorge Martínez Nieto,

Félix de la Fuente,

Raquel Guillén,

Natalia Acedo,

Cristina Serí,

Fernando Cava

Publication year - 2014

Publication title -

american journal of clinical pathology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.859

H-Index - 128

eISSN - 1943-7722

pISSN - 0002-9173

DOI - 10.1309/ajcppbq8ub1whxts

Subject(s) - microcytosis , mean corpuscular volume , anisocytosis , red blood cell distribution width , thalassemia , mean corpuscular hemoglobin , medicine , gastroenterology , iron deficiency anemia , mean corpuscular hemoglobin concentration , hemoglobin , receiver operating characteristic , anemia , iron deficiency

To analyze the differences not only in classic hematologic parameters but also in RBC subpopulations among δβ-thalassemia trait (δβ-TT), β-thalassemia trait (β-TT), and iron deficiency anemia (IDA) and to evaluate the role of fetal hemoglobin (HbF) in elevated RBC distribution width (RDW).

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