Severe Vitamin D Deficiency in a Patient with Sickle Cell Disease: a Case Study with Literature Review
Overview
Authors
Affiliations
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.
Response to Long-term Vitamin D Therapy for Bone Disease in Children With Sickle Cell Disease.
Williams K, Lee M, Licursi M, Brittenham G, Fennoy I J Pediatr Hematol Oncol. 2018; 40(6):458-461.
PMID: 29668535 PMC: 6059995. DOI: 10.1097/MPH.0000000000001155.
Shipton E, Shipton E Pain Res Treat. 2015; 2015:904967.
PMID: 26090221 PMC: 4427945. DOI: 10.1155/2015/904967.
Dougherty K, Bertolaso C, Schall J, Smith-Whitley K, Stallings V J Pediatr Hematol Oncol. 2015; 37(5):e308-15.
PMID: 25985241 PMC: 4474739. DOI: 10.1097/MPH.0000000000000355.