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

open access

Page views 441
Article views/downloads 261
Get Citation

Connect on Social Media

Connect on Social Media

Clinically diverse sickle cell disease influenced by genetic factors

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

Abstract

Not available

Article available in PDF format

View PDF Download PDF file

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