Pubertal Development in Girls with Beta Thalassaemia and Assessment of the Adequacy of Chelation Therapy: A Quasi-experimental Study
Introduction: Beta thalassaemia is the most prevalent hereditary autosomal disorder, significantly impacting endocrine function during pubertal development. The pathology is rooted in the excessive deposition of iron in vital organs. If left untreated, this condition leads to serious morbidity and m...
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| Principais autores: | , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
JCDR Research and Publications Private Limited
2024-03-01
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| Serier: | Journal of Clinical and Diagnostic Research |
| Fag: | |
| Online adgang: | https://www.jcdr.net/articles/PDF/19165/64430_CE[Ra1]_F(SL)_Ref_PAT(SL)_QC(SHK_IS))_PF1(RI_DK_OM)_PFA(RI_KM)_PN(KM).pdf |
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