| Literature DB >> 27365881 |
Avery Smith1, Barry Cooper1, Joseph Guileyardo1, Adan Mora1.
Abstract
Hemoglobin SE disease was first described during the 1950s as a relatively benign microcytosis, but increasing prevalence has revealed a predisposition towards vasoocclusive sickling. Recognition of SE hemoglobinopathies' potential complications is crucial so medical measures can be utilized to avoid multiorgan injury.Entities:
Year: 2016 PMID： 27365881 PMCID： PMC4900779 DOI： 10.1080/08998280.2016.11929447
Source DB: PubMed Journal: Proc (Bayl Univ Med Cent) ISSN： 0899-8280