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Investigation of the Relationship Between Fok1 and Col1A1 Gene Polymorphisms and Development of Treatment-Related Bone Complications in Children with Acute Lymphoblastic Leukemia

Melek ErdemÖzlem Tüfekçi GürocakSefa KızıldağŞebnem YılmazDeniz KızmazoğluBerna Eroğlu FilibeliHale Ören
Published in: Turkish journal of haematology : official journal of Turkish Society of Haematology (2018)
The development of therapy-induced bone mineral loss and osteonecrosis in children with ALL is frequent and the risk is especially higher in children aged ≥10 years and with vitamin D deficiency. The association between Col1A1 Sp1-binding site gene polymorphisms and osteonecrosis has to be assessed in a larger group of ALL survivors.
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