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Article

Transfusion requirements and complication rate in β-thalassemia intermedia due to heterozygous β-globin gene mutation and triplicated α-globin genes.

European journal of haematology - 1 Nov 2023

Bonello-Palot Nathalie, Benoit Audrey, Agouti Imane, Hamouda Ilyes, Brousse Valentine, Badens Catherine

Abstract excerpt

INTRODUCTION: The heterozygous condition for β-thalassemia mutation associated with an extra functional α-globin gene can produce a Thalassemia Intermedia (TI) phenotype. This genotype is the second in frequency in the French Thalassemia Registry NaThalY that prospectively collects laboratory and clinical data. MATERIALS AND METHODS: The present report analyses transfusion needs, iron overload (ferritin, hepatic...

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PMID: 37519097
DOI: 10.1111/ejh.14070

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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