Endocrine profile of β-thalassemia major patients followed from childhood to advanced adulthood in a tertiary care center

AIM: Chronic iron overload resulting from frequent transfusions, poor compliance to efficient chelation therapy and chronic liver disease is basically responsible for the most severe complications of thalassemia major (TM). Before conventional treatment, TM was entirely childhood disease with a very...

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Detalhes bibliográficos
Publicado no:Indian J Endocrinol Metab
Main Authors: De Sanctis, Vincenzo, Elsedfy, Heba, Soliman, Ashraf T., Elhakim, Ihab Zaki, Soliman, Nada A., Elalaily, Rania, Kattamis, Christos
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2016
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4911833/
https://ncbi.nlm.nih.gov/pubmed/27366710
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2230-8210.183456
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