Hepcidin mRNA and Endocrine Risk in β-Thalassemia

Beta-thalassemia major (BTM) is a severe transfusion-dependent disease complicated by secondary hemosiderosis, leading to organ damage in the heart, liver, and endocrine glands. Endocrine disorders are among the most frequent complications, significantly reducing quality of life.

Publication Details

Journal
Egyptian Society of Diabetes and Lipidology Journal
Published
2025-10-01
DOI
https://doi.org/10.21608/esdlj.2025.456297
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

Hepcidin mRNA and Endocrine Risk in β-Thalassemia

Egyptian Society of Diabetes and Lipidology Journal
Hemoglobinopathies and Related Disorders
article

Hepcidin mRNA and Endocrine Risk in β-Thalassemia

article en

Abstract

Beta-thalassemia major (BTM) is a severe transfusion-dependent disease complicated by secondary hemosiderosis, leading to organ damage in the heart, liver, and endocrine glands. Endocrine disorders are among the most frequent complications, significantly reducing quality of life.

Egyptian Society of Diabetes and Lipidology JournalVol. 5(2)
Openalex Percentile: Top 61%
Hemoglobinopathies and Related Disorders
DOIOpen Access PDFOpenAlex
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