Abstract
We report on a Pashtun family affected by haemoglobin D-Punjab/ β+-thalassemia to increase the awareness of the increasing prevalence of haemoglobinopathies among primary care physicians. We highlight the diagnostic approach of these conditions and the benefits of genetic counselling.
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CITATION STYLE
APA
Huits, R., Feyens, A. M., Lonneville, N., Peyrassol, X., Adam, A. S., Gulbis, B., & Van Esbroeck, M. (2022). Diagnosis and clinical relevance of co-inheritance of haemoglobin D-Punjab/β+-thalassemia traits in an immigrant Afghan family. Journal of Clinical Pathology, 75(12), 861–864. https://doi.org/10.1136/jclinpath-2021-208009
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