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The clinical utility of the PedsQL in adolescent and young adults with sickle cell disease

โœ Scribed by K. Lemanek


Book ID
116681871
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
33 KB
Volume
13
Category
Article
ISSN
1528-8447

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## Abstract Sickle cell disease (SCD) is a prevalent genetic disorder in which sickle hemoglobin leads to tissue hypoxia and adverse effects on bone. Published studies suggest that children with SCD often have undiagnosed osteopenia or osteoporosis. Minimal data exist on the prevalence of low bone