Vol 10, No 4 (2019)
Letter to the Editor
Published online: 2020-04-23

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Clinically diverse sickle cell disease influenced by genetic factors

Henu Kumar Verma1
Hematologia 2019;10(4):197-198.

Abstract

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References

  1. Lakkakula BV, Sahoo R, Verma H, et al. Pain management issues as part of the comprehensive care of patients with sickle cell disease. Pain Manag Nurs. 2018; 19(6): 558–572.
  2. Nongbri SR, Verma HK, Lakkakula BV, et al. Presence of atypical beta globin (HBB) gene cluster haplotypes in sickle cell anemia patients of India. Rev Bras Hematol Hemoter. 2017; 39(2): 180–182.
  3. Nishank SS, Singh MP, Yadav R, et al. Endothelial nitric oxide synthase gene polymorphism is associated with sickle cell disease patients in India. J Hum Genet. 2013; 58(12): 775–779.
  4. Alagbe AE, Olaniyi JA, Aworanti OW. Adult Sickle Cell Anaemia Patients in Bone Pain Crisis have Elevated Pro-Inflammatory Cytokines. Mediterr J Hematol Infect Dis. 2018; 10(1): e2018017.
  5. Verma H, Mishra H, Khodiar PK, et al. NOS3 27-bp and IL4 70-bp VNTR Polymorphisms Do Not Contribute to the Risk of Sickle Cell Crisis. Turk J Haematol. 2016; 33(4): 365–366.
  6. Bhanushali AA, Patra PK, Nair D, et al. Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients. Blood Cells Mol Dis. 2015; 54(1): 4–8.
  7. Rumaney MB, Ngo Bitoungui VJ, Vorster AA, et al. The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival. PLoS One. 2014; 9(6): e100516.



Hematology in Clinical Practice