Hemoglobinopathy in India

Clinica Chimica Acta

Volumn 444, Issue , 2015, Pages 229-233

  Iyer, Sandhya ^a   Sakhare, Suhas ^a   Sengupta, Caesar ^a   Velumani, A ^a  

^a Thyrocare Technologies Ltd   (India)

Author keywords

Anemia; Hemoglobinopathy; India; Thalassemia

Indexed keywords

AFRICAN AMERICAN; ALPHA THALASSEMIA; ASIAN INDIAN; BETA THALASSEMIA; BLOOD CELL COUNT; CAPILLARY ELECTROPHORESIS; COHORT ANALYSIS; CONTROLLED STUDY; GENE MUTATION; GENETIC VARIABILITY; HEMOGLOBINOPATHY; HETEROZYGOSITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; INDIA; INDIAN; IRON DEFICIENCY ANEMIA; MAJOR CLINICAL STUDY; PREVALENCE; PRIORITY JOURNAL; REVIEW; SICKLE CELL TRAIT; GENETIC VARIATION; GENETICS; HEMOGLOBINOPATHIES;

HEMOGLOBIN;

CHROMATOGRAPHY, HIGH PRESSURE LIQUID; COHORT STUDIES; ELECTROPHORESIS, CAPILLARY; GENETIC VARIATION; HEMOGLOBINOPATHIES; HEMOGLOBINS; HUMANS; INDIA;

EID: 84924217274     PISSN: 00098981     EISSN: 18733492     Source Type: Journal    
DOI: 10.1016/j.cca.2015.02.033     Document Type: Review

References (17)

1. Hoyer J.D. Hemoglobinopathies: the how, why and what. ASCP annual meeting 2011.
2. Data adopted from the online HbVar database. Accessed on 5th February 2015.
3. Gorakshakar A.C. Epidemiology of sickle hemoglobin in India Available from:. http://www.rmrct.org/files_rmrc_web/centre's_publications/nsth_06/nsth06_14.ac.gorakshakar.pdf.
4. Clarke G.M., Higgins T.N. Laboratory investigation of hemoglobinopathies and thalassemias: review and update. Clin Chem 2000, 46(8(B)):1284-1290.
5. Chandrashekar V., Soni M. Hemoglobin disorders in South India. ISRN hematol 2011, [Article ID 748939]. 10.5402/2011/748939.
6. Balgir R.S. Genetic epidemiology of the three predominant abnormal hemoglobins in India. J Assoc Physicians India 1996, 44(1):25-28.
7. Rao S., Kar R., Gupta S.K., Chopra A., Saxena R. Spectrum of hemoglobinopathies diagnosed by cation exchange HPLC & modulating effects of nutritional deficiency anaemias from North India. Indian J Med Res 2009, 132:519-519.
8. Rahbar S., Hemoglobin D. Iran: 2 22 glutamic acid leads to glutamine (B4). Br J Haematol 1973, 24(1):31-35.
9. Keren D.F. Clinical evaluation of hemoglobinopathies: Part II. Structural changes. Warde Med Lab 2003, 14(3).
10. Das K., Dhas P., Sahu P.N., Rao V.R., Mohanty D. Abnormal hemoglobins (HbD and HbQ-India) and β-thalassemia among the Indian Sindhis. Hereditary Genet 2013, [S1:008]. 10.4172/2161-1041.S1-008.
11. Blackwell R.Q., Wong H.B., Wang C.L., Weng M.I., Liu C.S. Hemoglobin J Meerut: α 120 Ala leads to Glu. Biochim Biophys Acta 1974, 351:7-12.
12. Ne-Win, Harano K., Harano T., et al. Hb Constant Spring [alpha 142, Term --> Gln (TAA>CAA) in alpha 2)] in the alpha-thalassemia of anemic patients in Myanmar. Hemoglobin 2008, 32(5):454-461.
13. An online article on "Hemoglobin Lepore" by European Network for Rare and Congenital Anemias. Accessed on 5th February 2015.
14. Ingle J., Adewoye A., Dewan R., et al. Hb Hope [β136(H14)Gly→Asp (GGT→GAT)]: interactions with HbS [β6(A3)Glu→Val (GAG→GTG)], other variant hemoglobins and thalassemia. Hemoglobin 2004, 28(4):277-285.
15. Bunn F.H., Forget B.G. Hemoglobin: molecular, genetic and clinical aspects 1986, 425-427. WB Saunders, Philadelphia (PA).
16. Brant A. Hemoglobinopathy & thalassemia detection: traditional method-capillary electrophoresis technology. Sebia® electrophoresis newsletter 2010, 1:1-4. 11.
17. Urade B.P. Sickle cell gene (HbS) scenario in Tribal India. J Health Med Inform 2012, 3:114.