Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis Patients.
Camelia AlkhzouzGeorgiana CabauCecilia LazeaCarmen AsavoaieSimona BucerzanAndreea Manuela MireaMarius FarcasMaria Miclaus JnrRadu PoppDiana MicleaPublished in: Pharmacogenomics and personalized medicine (2021)
In MPS patients, vitamin D deficiency is observed, as it is in some patients with secondary hyperparathyroidism, which indicates vitamin D supplementation to protect bone metabolism. There are no obvious correlations between VDR polymorphism and bone metabolism in MPS patients.