Endocrine and metabolic complications in children and adolescents with Sickle Cell Disease: an Italian cohort study

BACKGROUND: Children with Sickle Cell Disease (SCD) show endocrine complications and metabolic alterations. The physiopathology of these conditions is not completely understood: iron overload due to chronic transfusions, ischemic damage, and inflammatory state related to vaso-occlusive crises may be...

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Detalles Bibliográficos
Autores principales: Mandese, V., Bigi, E., Bruzzi, P., Palazzi, G., Predieri, B., Lucaccioni, L., Cellini, M., Iughetti, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371531/
https://www.ncbi.nlm.nih.gov/pubmed/30744584
http://dx.doi.org/10.1186/s12887-019-1423-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371531/
https://www.ncbi.nlm.nih.gov/pubmed/30744584
http://dx.doi.org/10.1186/s12887-019-1423-9

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