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Lack of biochemical hypogonadism in elderly Arab males with low bone mineral density disease

✍ Scribed by Haider M. Al Attia; Krishnasamy Jaysundaram; Fouad Saraj


Publisher
Springer
Year
2009
Tongue
English
Weight
178 KB
Volume
30
Category
Article
ISSN
0172-8172

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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