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American Society of Hematology 2019 guidelines for sickle cell disease: cardiopulmonary and kidney disease.

07:00 EST 10th December 2019 | BioPortfolio

Summary of "American Society of Hematology 2019 guidelines for sickle cell disease: cardiopulmonary and kidney disease."

Prevention and management of end-organ disease represent major challenges facing providers of children and adults with sickle cell disease (SCD). Uncertainty and variability in the screening, diagnosis, and management of cardiopulmonary and renal complications in SCD lead to varying outcomes for affected individuals.

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This article was published in the following journal.

Name: Blood advances
ISSN: 2473-9537
Pages: 3867-3897

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Medical and Biotech [MESH] Definitions

One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia.

An abnormal hemoglobin resulting from the substitution of valine for glutamic acid at position 6 of the beta chain of the globin moiety. The heterozygous state results in sickle cell trait, the homozygous in sickle cell anemia.

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