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Severe Vitamin D Deficiency in a Patient with Sickle Cell Disease: a Case Study with Literature Review

Overview
Specialty Pediatrics
Date 2013 Nov 27
PMID 24276034
Citations 3
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Abstract

Purpose: Vitamin D is essential for the normal absorption of calcium and to maintain calcium homeostasis. Vitamin D deficiency results in rickets, osteomalacia, and bony changes in the spine. Sickle cell disease patients are at an increased risk of vitamin D deficiency.

Case Presentation: We describe a case of severe vitamin D deficiency and response to vitamin D supplementation in a patient with sickle cell disease.

Conclusions: Currently, there are no recommendations for calcium and vitamin D supplementation in sickle cell patients. Vitamin D deficiency in these patients may be due to poor absorption.

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Williams K, Lee M, Licursi M, Brittenham G, Fennoy I J Pediatr Hematol Oncol. 2018; 40(6):458-461.

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Vitamin D and Pain: Vitamin D and Its Role in the Aetiology and Maintenance of Chronic Pain States and Associated Comorbidities.

Shipton E, Shipton E Pain Res Treat. 2015; 2015:904967.

PMID: 26090221 PMC: 4427945. DOI: 10.1155/2015/904967.


Safety and Efficacy of High-dose Daily Vitamin D3 Supplementation in Children and Young Adults With Sickle Cell Disease.

Dougherty K, Bertolaso C, Schall J, Smith-Whitley K, Stallings V J Pediatr Hematol Oncol. 2015; 37(5):e308-15.

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