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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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Detalles Bibliográficos
Autores principales: De Sanctis, Vincenzo, Elsedfy, Heba, Soliman, Ashraf T., Elhakim, Ihab Zaki, Soliman, Nada A., Elalaily, Rania, Kattamis, Christos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4911833/
https://www.ncbi.nlm.nih.gov/pubmed/27366710
http://dx.doi.org/10.4103/2230-8210.183456