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The increased survival in SCD brings to the front previously unrecognized complications including pulmonary hypertension, silent cerebral infarcts and also reproductive dysfunction. Adolescents and young adults (AYAs) have age-related psychosocial needs in their transition from the pediatric health care environment to the adult system. In this review we present the uniquely age-related medical issues facing the AYA thalassemia and SCD cohort in their transition into adulthood.<\/jats:p>","DOI":"10.1159\/000360235","type":"journal-article","created":{"date-parts":[[2014,9,10]],"date-time":"2014-09-10T06:58:13Z","timestamp":1410332293000},"page":"340-347","source":"Crossref","is-referenced-by-count":8,"title":["Thalassemia Major and Sickle Cell Disease in Adolescents and Young 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