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...

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Detalles Bibliográficos
Autores principales: Ayan, Durmus, Kirbiyik, Ozgur, Ozyilmaz, Berk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Istanbul Medeniyet University 2019
Materias:
Case Report
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

Internet

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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