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Russo, Giovanna; De Franceschi, Lucia; Colombatti, Raffaella; Rigano, Paolo; Perrotta, Silverio; Voi, Vincenzo; Palazzi, Giovanni; Fidone, Carmelo; Quota, Alessandra; Graziadei, Giovanna; Pietrangelo, Antonello; Pinto, Valeria; Ruffo, Giovan Battista; Sorrentino, Francesco; Venturelli, Donatella; Casale, Maddalena; Ferrara, Francesca; Sainati, Laura; Cappellini, Maria Domenica; Piga, Antonio; Maggio, Aurelio; Forni, Gian Luca
Orphanet journal of rare diseases, 05/2019, Letnik: 14, Številka: 1Journal Article
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality of hemoglobin called sickle hemoglobin (HbS). Clinical manifestations of SCD are mainly characterized by chronic hemolysis and acute vaso-occlusive crisis, which are responsible for severe acute and chronic organ damage. SCD is widespread in sub-Saharan Africa, in the Middle East, Indian subcontinent, and some Mediterranean regions. With voluntary population migrations, people harboring the HbS gene have spread globally. In 2006, the World Health Organization recognized hemoglobinopathies, including SCD, as a global public health problem and urged national health systems worldwide to design and establish programs for the prevention and management of SCD. Herein we describe the historical experience of the network of hemoglobinopathy centers and their approach to SCD in Italy, a country where hemoglobinopathies have a high prevalence and where SCD, associated with different genotypes including ß-thalassemia, is present in the native population.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Povezave do osebnih bibliografij avtorjev | Povezave do podatkov o raziskovalcih v sistemu SICRIS |
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Vir: Osebne bibliografije
in: SICRIS
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