HEMOGLOBINOPATHY

Journal Title: International scientific journal Science and Innovation - Year 2024, Vol 3, Issue 4

Abstract

Hemoglobinopathies are a group of severe hereditary blood diseases caused by a violation of the structure of hemoglobin or a decrease in the synthesis of one or more globin chains. The clinical picture is extremely varied. Common symptoms are hemolytic anemia, enlarged spleen, and bone damage. Diagnosis is carried out using peripheral blood smear microscopy, hemoglobin electrophoresis, and genetic studies. For treatment, transfusions of blood components, hydroxyurea preparations, and infusion therapy are used. In severe patients, splenectomy and stem cell allotransplantation are performed.

Authors and Affiliations

Sultonova Mukhlisa, Sultonova Maftuna, Islomjonova Iroda, Mirzakeldiyeva Khatira, Naimov Bunyod

Keywords

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  • EP ID EP735587
  • DOI 10.5281/zenodo.11113974
  • Views 23
  • Downloads 0

How To Cite

Sultonova Mukhlisa, Sultonova Maftuna, Islomjonova Iroda, Mirzakeldiyeva Khatira, Naimov Bunyod (2024). HEMOGLOBINOPATHY. International scientific journal Science and Innovation, 3(4), -. https://europub.co.uk/articles/-A-735587