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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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Detalles Bibliográficos
Autores principales:	Dhouib, Naouel Guirat, Ben Khaled, Monia, Ouederni, Monia, Besbes, Habib, Kouki, Ridha, Mellouli, Fethi, Bejaoui, Mohamed
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Università Cattolica del Sacro Cuore 2018
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937976/ https://www.ncbi.nlm.nih.gov/pubmed/29755708 http://dx.doi.org/10.4084/MJHID.2018.031

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