Article

Genetic Approach in Diagnosis and Follow-Up of Patients with Thalassemia: A Comprehensive Narrative Review

2026-06-15

Abstract excerpt

<h4>Background: </h4> Thalassemia represents the world’s most prevalent inherited hemoglobin disorder, affecting approximately 4.4 per 10,000 live births globally. Accurate genetic characterization is indispensable both for definitive diagnosis and for lifetime clinical monitoring. The past two decades have witnessed a paradigm shift from conventional protein-based assays toward comprehensive molecular techniques,...

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Literature Corpus work: 095a8569-07b0-5792-ad7b-9643148ea356
DOI: 10.20944/preprints202606.1060.v1

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