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01.12.2017 | Original Article

Evaluation of bone mineral density in children with sickle-cell anemia and its associated factors in the south of Iran: a case-control study

verfasst von: Mohammad Reza Bordbar, Sezaneh Haghpanah, Tahereh Zarei, Mohammad Hossein Dabbaghmanesh, Gholamhossein Ranjbar Omrani, Forough Saki

Erschienen in: Archives of Osteoporosis | Ausgabe 1/2017

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Abstract

Summary

Sickle-cell anemia is a hereditary hemoglobin disorder among children. We showed that the low bone mass is prevalent among these children, and it has a negative association with hemoglobin. In spite of using supplementary 200 IU/day vitamin D, 59.6% of children with sickle-cell anemia are vitamin D deficient. We suggest that early diagnosis and treatment of this problem could improve the bone health in them.

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Titel: Evaluation of bone mineral density in children with sickle-cell anemia and its associated factors in the south of Iran: a case-control study
verfasst von: Mohammad Reza Bordbar
Sezaneh Haghpanah
Tahereh Zarei
Mohammad Hossein Dabbaghmanesh
Gholamhossein Ranjbar Omrani
Forough Saki
Publikationsdatum: 01.12.2017
Verlag: Springer London
Erschienen in: Archives of Osteoporosis / Ausgabe 1/2017
Print ISSN: 1862-3522
Elektronische ISSN: 1862-3514
DOI: https://doi.org/10.1007/s11657-017-0364-x

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