Growth and Endocrine Function in Tunisian Thalassemia Major Patients

β-thalassemia major (β–TM) is among the most common hereditary disorders imposing high expenses on health-care system worldwide. The patient’s survival is dependent on lifetime blood transfusion which leads to iron overload and its toxicity in various organs including endocrine glands. This article...

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Detalhes bibliográficos
Publicado no:Mediterr J Hematol Infect Dis
Main Authors: Dhouib, Naouel Guirat, Ben Khaled, Monia, Ouederni, Monia, Besbes, Habib, Kouki, Ridha, Mellouli, Fethi, Bejaoui, Mohamed
Formato: Artigo
Idioma:Inglês
Publicado em: Università Cattolica del Sacro Cuore 2018
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5937976/
https://ncbi.nlm.nih.gov/pubmed/29755708
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4084/MJHID.2018.031
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