Hemoglobinopathies constitute a major health problem worldwide, with a high carrier frequency, particularly in certain regions where malaria has been endemic. These disorders are characterized by a vast clinical and hematological phenotypic heterogeneity. Over 1,200 different genetic alterations that affect the DNA sequence of the human α-like (HBZ, HBA2, HBA1, and HBQ1) and β-like (HBE1, HBG2, HBG1, HBD, and HBB) globin genes are mainly responsible for the observed clinical heterogeneity. These mutations, together with detailed information about the resulting phenotype, are documented in the globin locus-specific HbVar database. Family studies and comprehensive hematological analyses provide useful insights for accurately diagnosing thalassemia at the DNA level. For this purpose, numerous techniques can provide accurate, rapid, and cost-effective identification of the underlying genetic defect in affected individuals. The aim of this article is to review the diverse methodological and technical platforms available for the molecular diagnosis of inherited disorders, using thalassemia and hemoglobinopathies as a model. This article also attempts to shed light on issues closely related to thalassemia diagnostics, such as prenatal and preimplantation genetic diagnoses and genetic counseling, for better-quality disease management.

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doi.org/10.1002/humu.20225, hdl.handle.net/1765/69158
Human Mutation
Biophysical Genomics, Department Cell Biology & Genetics

Patrinos, G., Kollia, P., & Papadakis, M. (2005). Molecular diagnosis of inherited disorders: Lessons from hemoglobinopathies. Human Mutation (Vol. 26, pp. 399–412). doi:10.1002/humu.20225