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Evaluation of Clinical, Laboratory Characteristics of Hemoglobin H Disease Patients from 2002 to 2022 Referred to Thalassemia Center, Bu-Ali Sina Hospital in Sari North of Iran

2024-02-28

Abstract excerpt

<title>Abstract</title> <p>Background Alpha Thalassemia is a common hereditary anemia which results from decreased alpha-globin production. The clinical manifestations of these genetic abnormalities range from a silent carrier state, to fatal hydrops fetalis. Hemoglobin H disease (HbH disease) is type of α-thalassemia which is affect three of the four α-globin genes. Methods This study was conducted on all pati...

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Literature Corpus work: 3361b159-8c8a-559e-b5e7-7012aba48f78
DOI: 10.21203/rs.3.rs-3974063/v1

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