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Heterozygous Beta Chain Variant Hemoglobin Pusan: A Rare Case Report in Turkish Population
The case, detected during routine thalassemia (hemoglobin variant) screening, was a 25-year-old male patient of Turkish origin. Physical examination revealed no abnormal findings. Laboratory findings did not reveal any signs of anemia (iron deficiency, B12 deficiency, etc.). However, when the hemogl...
Autores principales: | Ayan, Durmus, Kirbiyik, Ozgur, Ozyilmaz, Berk |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Istanbul Medeniyet University
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433718/ https://www.ncbi.nlm.nih.gov/pubmed/32821467 http://dx.doi.org/10.5222/MMJ.2019.10476 |
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