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Volumn 134, Issue 10, 2011, Pages 498-506

Haemoglobinopathies in Southeast Asia

Author keywords

thalassaemia; thalassaemia; Haemoglobin (Hb) E; Hb constant spring (CS)

Indexed keywords

ALPHA GLOBIN; DEFEROXAMINE; FERRITIN; HEMOGLOBIN E; HEMOGLOBIN H; IRON;

EID: 80455127464     PISSN: 09715916     EISSN: 09715916     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (185)

References (65)
  • 2
    • 0344725589 scopus 로고
    • Hemoglobinopathies in Southeast Asia
    • Bowman JE, editor, New York: Elsevier
    • Wasi P. Hemoglobinopathies in Southeast Asia. In: Bowman JE, editor. Distribution and evolution of hemoglobin and globin Loci. New York: Elsevier; 1983. p. 179-203.
    • (1983) Distribution and Evolution of Hemoglobin and Globin Loci , pp. 179-203
    • Wasi, P.1
  • 3
    • 0023112573 scopus 로고
    • Hemoglobinopathies in Southeast Asia
    • Fucharoen S, Winichagoon P. Hemoglobinopathies in Southeast Asia. Hemoglobin 1987; 11: 65-8.
    • (1987) Hemoglobin , vol.11 , pp. 65-68
    • Fucharoen, S.1    Winichagoon, P.2
  • 6
    • 0024996741 scopus 로고
    • The Molecular basis of β-thalassemia in Thailand: Application to prenatal diagnosis
    • Thein SL, Winichagoon P, Hesketh C, Best S, Fucharoen S, Wasi P, et al. The Molecular basis of β-thalassemia in Thailand: Application to prenatal diagnosis. Am J Hum Genet 1990; 47: 369-75.
    • (1990) Am J Hum Genet , vol.47 , pp. 369-375
    • Thein, S.L.1    Winichagoon, P.2    Hesketh, C.3    Best, S.4    Fucharoen, S.5    Wasi, P.6
  • 12
    • 0023789105 scopus 로고
    • Characterization of two deletions that remove the entire human α-globin gene complex (--THAI and --FIL)
    • Fischel-Ghodsian N, Vickers MA, Seip M, Winichagoon P, Higgs DR. Characterization of two deletions that remove the entire human α-globin gene complex (--THAI and --FIL). Br J Haematol 1988; 70: 233-8.
    • (1988) Br J Haematol , vol.70 , pp. 233-238
    • Fischel-Ghodsian, N.1    Vickers, M.A.2    Seip, M.3    Winichagoon, P.4    Higgs, D.R.5
  • 13
    • 29744458124 scopus 로고    scopus 로고
    • Understanding alpha-globin gene regulation: Aiming to improve the management of thalassemia
    • Higgs DR, Garrick D, Anguita E, De Gobbi M, Hughes J, Muers M, et al. Understanding alpha-globin gene regulation: aiming to improve the management of thalassemia. Ann NY Acad Sci 2005; 1054: 92-102.
    • (2005) Ann NY Acad Sci , vol.1054 , pp. 92-102
    • Higgs, D.R.1    Garrick, D.2    Anguita, E.3    de Gobbi, M.4    Hughes, J.5    Muers, M.6
  • 14
    • 33646434782 scopus 로고    scopus 로고
    • A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element
    • Viprakasit V, Harteveld CL, Ayyub H, Stanley JS, Giordano PC, Wood WG, et al. A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element. Blood 2006; 107: 3811-2.
    • (2006) Blood , vol.107 , pp. 3811-3812
    • Viprakasit, V.1    Harteveld, C.L.2    Ayyub, H.3    Stanley, J.S.4    Giordano, P.C.5    Wood, W.G.6
  • 18
    • 0022978460 scopus 로고
    • Human α-globin gene expression. The dominant role of the α2-locus in mRNA and protein synthesis
    • Liebhaber SA, Cash FE, Ballas SK. Human α-globin gene expression. The dominant role of the α2-locus in mRNA and protein synthesis. J Biol Chem 1986; 261: 15327-33.
    • (1986) J Biol Chem , vol.261 , pp. 15327-15333
    • Liebhaber, S.A.1    Cash, F.E.2    Ballas, S.K.3
  • 19
    • 0026670290 scopus 로고
    • Translation inhibition by an mRNA coding region secondary structure is determined by its proximity to the AUG initiation codon
    • Liebhaber SA, Cash F, Eshleman SS. Translation inhibition by an mRNA coding region secondary structure is determined by its proximity to the AUG initiation codon. J Mol Biol 1992; 226: 609-21.
    • (1992) J Mol Biol , vol.226 , pp. 609-621
    • Liebhaber, S.A.1    Cash, F.2    Eshleman, S.S.3
  • 21
    • 1342302434 scopus 로고    scopus 로고
    • Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease
    • Viprakasit V, Tanphaichitr VS, Veerakul G, Chinchang W, Petrarat S, Pung-Amritt P, et al. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease. Am J Hematol 2004; 75: 157-63.
    • (2004) Am J Hematol , vol.75 , pp. 157-163
    • Viprakasit, V.1    Tanphaichitr, V.S.2    Veerakul, G.3    Chinchang, W.4    Petrarat, S.5    Pung-Amritt, P.6
  • 24
    • 0023465373 scopus 로고
    • In vivo induction of intraerythrocytic inclusion bodies in hemoglobin H disease: An electron microscopic study
    • Chinprasertsuk S, Piankijagum A, Wasi P. In vivo induction of intraerythrocytic inclusion bodies in hemoglobin H disease: an electron microscopic study. Birth Defects 1988; 23: 317-26.
    • (1988) Birth Defects , vol.23 , pp. 317-326
    • Chinprasertsuk, S.1    Piankijagum, A.2    Wasi, P.3
  • 25
    • 0023463016 scopus 로고
    • Differences between two types of Hb H disease, α-thalassemia 1/α-thalassemia 2 and α-thalassemia 1/Hb Constant Spring
    • Fucharoen S, Winichagoon P, Pootrakul P, Piankijagum A, Wasi P. Differences between two types of Hb H disease, α-thalassemia 1/α-thalassemia 2 and α-thalassemia 1/Hb Constant Spring. Birth Defects 1988; 23: 309-15.
    • (1988) Birth Defects , vol.23 , pp. 309-315
    • Fucharoen, S.1    Winichagoon, P.2    Pootrakul, P.3    Piankijagum, A.4    Wasi, P.5
  • 26
    • 0023806677 scopus 로고
    • Different forms of Hb H disease in the Chinese
    • Chan V, Chan TK, Todd D. Different forms of Hb H disease in the Chinese. Hemoglobin 1988; 12: 499-507.
    • (1988) Hemoglobin , vol.12 , pp. 499-507
    • Chan, V.1    Chan, T.K.2    Todd, D.3
  • 27
    • 0037305250 scopus 로고    scopus 로고
    • Hemoglobin H disease: Not necessarily a benign disorder
    • Chui DH, Fucharoen S, Chan V. Hemoglobin H disease: not necessarily a benign disorder. Blood 2003; 101: 791-800.
    • (2003) Blood , vol.101 , pp. 791-800
    • Chui, D.H.1    Fucharoen, S.2    Chan, V.3
  • 29
    • 0019169855 scopus 로고
    • Levels of haemoglobin H and proportions of red cells with inclusion bodies in the two types of haemoglobin H disease
    • Winichagoon P, Adirojnanon P, Wasi P. Levels of haemoglobin H and proportions of red cells with inclusion bodies in the two types of haemoglobin H disease. Br J Haematol 1980; 46: 507-9.
    • (1980) Br J Haematol , vol.46 , pp. 507-509
    • Winichagoon, P.1    Adirojnanon, P.2    Wasi, P.3
  • 30
    • 0025937911 scopus 로고
    • Hemoglobin Constant Spring in Bangkok: Molecular screening by selective enzymatic amplification of the α2-globin gene
    • Thonglairoam V, Winichagoon P, Fucharoen S, Tanphaichitr VS, Pung-Amritt P, Embury SH, et al. Hemoglobin Constant Spring in Bangkok: Molecular screening by selective enzymatic amplification of the α2-globin gene. Am J Hematol 1991; 38: 277-80.
    • (1991) Am J Hematol , vol.38 , pp. 277-280
    • Thonglairoam, V.1    Winichagoon, P.2    Fucharoen, S.3    Tanphaichitr, V.S.4    Pung-Amritt, P.5    Embury, S.H.6
  • 31
    • 0023904470 scopus 로고
    • EF Bart's disease: Interaction of the abnormal α- and β-globin genes
    • Fucharoen S, Winichagoon P, Thonglairoam V, Wasi P. EF Bart's disease: interaction of the abnormal α- and β-globin genes. Eur J Haematol 1988; 40: 75-8.
    • (1988) Eur J Haematol , vol.40 , pp. 75-78
    • Fucharoen, S.1    Winichagoon, P.2    Thonglairoam, V.3    Wasi, P.4
  • 36
    • 77952634429 scopus 로고    scopus 로고
    • Epidemiology of β-thalassaemia in Western India: Mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat
    • Colah R, Gorakshakar A, Phanasgaonkar S, D'Souza E, Nadkarni A, Surve R, et al. Epidemiology of β-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat. Br J Haematol 2010; 149: 739-47.
    • (2010) Br J Haematol , vol.149 , pp. 739-747
    • Colah, R.1    Gorakshakar, A.2    Phanasgaonkar, S.3    D'souza, E.4    Nadkarni, A.5    Surve, R.6
  • 37
    • 0020033690 scopus 로고
    • Instability of βE-messenger RNA during erythroid cell maturation in hemoglobin E homozygotes
    • Traeger J, Winichagoon P, Wood WG. Instability of βE-messenger RNA during erythroid cell maturation in hemoglobin E homozygotes. J Clin Invest 1982; 69: 1050-3.
    • (1982) J Clin Invest , vol.69 , pp. 1050-1053
    • Traeger, J.1    Winichagoon, P.2    Wood, W.G.3
  • 39
    • 57949106014 scopus 로고    scopus 로고
    • Molecular, hematological and clinical aspects of thalassemia major and thalassaemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand
    • Nuntakarn L, Fucharoen S, Fucharoen G, Sanchaisuriya K, Jetsrisuparb A, Wiangnon S. Molecular, hematological and clinical aspects of thalassemia major and thalassaemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand. Blood Cells Mol Dis 2009; 42: 32-5.
    • (2009) Blood Cells Mol Dis , vol.42 , pp. 32-35
    • Nuntakarn, L.1    Fucharoen, S.2    Fucharoen, G.3    Sanchaisuriya, K.4    Jetsrisuparb, A.5    Wiangnon, S.6
  • 40
    • 0019814079 scopus 로고
    • Serum ferritin levels in thalassemias and the effect of splenectomy
    • Pootrakul P, Vongsmasa V, La-ongpanich P, Wasi P. Serum ferritin levels in thalassemias and the effect of splenectomy. Acta Haematol 1981; 66: 244-50.
    • (1981) Acta Haematol , vol.66 , pp. 244-250
    • Pootrakul, P.1    Vongsmasa, V.2    La-Ongpanich, P.3    Wasi, P.4
  • 42
    • 0034307683 scopus 로고    scopus 로고
    • A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in Thai patients with thalassemia
    • Pootrakul P, Sirankapracha P, Hemsorach S, Moungsub W, Kumbunlue R, Piangitjagum A, et al. A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in Thai patients with thalassemia. Blood 2000; 96: 2606-12.
    • (2000) Blood , vol.96 , pp. 2606-2612
    • Pootrakul, P.1    Sirankapracha, P.2    Hemsorach, S.3    Moungsub, W.4    Kumbunlue, R.5    Piangitjagum, A.6
  • 46
    • 77949274495 scopus 로고    scopus 로고
    • A genome-wide association identified the common genetic variants influence disease severity in β-thalassemia/hemoglobin E
    • Nuinoon M, Makarasara W, Mushiroda T, Setianingsih I, Wahidiyat PA, Sripichai O, et al. A genome-wide association identified the common genetic variants influence disease severity in β-thalassemia/hemoglobin E. Hum Genet 2010; 127: 303-14.
    • (2010) Hum Genet , vol.127 , pp. 303-314
    • Nuinoon, M.1    Makarasara, W.2    Mushiroda, T.3    Setianingsih, I.4    Wahidiyat, P.A.5    Sripichai, O.6
  • 47
    • 0022006714 scopus 로고
    • DNA sequence variation associated with elevated fetal Gg globin production
    • Gilman JG, Huisman THJ. DNA sequence variation associated with elevated fetal Gg globin production. Blood 1985; 66: 783-7.
    • (1985) Blood , vol.66 , pp. 783-787
    • Gilman, J.G.1    Huisman, T.H.J.2
  • 48
    • 0346497365 scopus 로고
    • Common haplotype dependency of high Gα-globin gene expression and high Hb F levels in β-thalassemia and sickle cell anemia patients
    • Labie D, Pagnier J, Lapoumeroulie C, Rouabhi F, Dunda-Belkhodja O, Chardin P, et al. Common haplotype dependency of high Gα-globin gene expression and high Hb F levels in β-thalassemia and sickle cell anemia patients. Proc Natl Acad Sci USA 1985; 82: 2111-4.
    • (1985) Proc Natl Acad Sci USA , vol.82 , pp. 2111-2114
    • Labie, D.1    Pagnier, J.2    Lapoumeroulie, C.3    Rouabhi, F.4    Dunda-Belkhodja, O.5    Chardin, P.6
  • 49
    • 34547450531 scopus 로고    scopus 로고
    • Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults
    • Thein SL, Menzel S, Peng X, Best S, Jiang J Close J, et al. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults. Proc Natl Acad Sci USA 2007; 104: 11346-51.
    • (2007) Proc Natl Acad Sci USA , vol.104 , pp. 11346-11351
    • Thein, S.L.1    Menzel, S.2    Peng, X.3    Best, S.4    Jiang, J.5    Close, J.6
  • 50
    • 50149117726 scopus 로고    scopus 로고
    • DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
    • Lettre G, Sankaran VG, Bezerra MA, Araujo AS, Uda M, Sanna S, et al. DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proc Natl Acad Sci USA 2008; 105: 11869-74.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 11869-11874
    • Lettre, G.1    Sankaran, V.G.2    Bezerra, M.A.3    Araujo, A.S.4    Uda, M.5    Sanna, S.6
  • 51
    • 34748864128 scopus 로고    scopus 로고
    • A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15
    • Menzel S, Garner C, Gut I, Masuda F, Yamaguchi M, Heath S, et al. A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. Nat Genet 2007; 39: 1197-9.
    • (2007) Nat Genet , vol.39 , pp. 1197-1199
    • Menzel, S.1    Garner, C.2    Gut, I.3    Masuda, F.4    Yamaguchi, M.5    Heath, S.6
  • 52
    • 0026557081 scopus 로고
    • Variation of HbF and F-cell number with the G-gamma Xmn I (C-T) polymorphism in normal individuals
    • Sampietro M, Thein SL, Contreras M, Pazmany L. Variation of HbF and F-cell number with the G-gamma Xmn I (C-T) polymorphism in normal individuals. Blood 1992; 79: 832-3.
    • (1992) Blood , vol.79 , pp. 832-833
    • Sampietro, M.1    Thein, S.L.2    Contreras, M.3    Pazmany, L.4
  • 53
    • 0023797934 scopus 로고
    • The WHO control program for hereditary anemia
    • Kuliev AM. The WHO control program for hereditary anemia. Birth Defects 1988; 23: 383-94.
    • (1988) Birth Defects , vol.23 , pp. 383-394
    • Kuliev, A.M.1
  • 54
    • 0023673669 scopus 로고
    • Control of β-thalassemia in Sardinia
    • Cao A, Rosatelli C. Control of β-thalassemia in Sardinia. Birth Defects 1988; 23: 395-404.
    • (1988) Birth Defects , vol.23 , pp. 395-404
    • Cao, A.1    Rosatelli, C.2
  • 56
    • 0025187273 scopus 로고
    • Cyprus: Thalassemia programme
    • Angastiniotis M. Cyprus: thalassemia programme. Lancet 1990; 2: 1119-20.
    • (1990) Lancet , vol.2 , pp. 1119-1120
    • Angastiniotis, M.1
  • 60
    • 53749101257 scopus 로고    scopus 로고
    • Rapid diagnosis of thalassemias and other hemoglobinopathies by capillary electrophoresis system
    • Winichagoon P, Svasti S, Munkongdee T, Chaiya W, Boonmongkol P, Chantrakul N, et al. Rapid diagnosis of thalassemias and other hemoglobinopathies by capillary electrophoresis system. Transl Res 2008; 152: 178-84.
    • (2008) Transl Res , vol.152 , pp. 178-184
    • Winichagoon, P.1    Svasti, S.2    Munkongdee, T.3    Chaiya, W.4    Boonmongkol, P.5    Chantrakul, N.6
  • 61
    • 0042406372 scopus 로고
    • Dichlorophenolindophenol (DCIP) precipitation test: A new screening test for Hb E and H
    • Kulapongs P, Sanguansermsri T, Mertz G, Tawarat S. Dichlorophenolindophenol (DCIP) precipitation test: a new screening test for Hb E and H. Pediatr Soc Thailand 1976; 15: 1-7.
    • (1976) Pediatr Soc Thailand , vol.15 , pp. 1-7
    • Kulapongs, P.1    Sanguansermsri, T.2    Mertz, G.3    Tawarat, S.4
  • 62
    • 0019837519 scopus 로고
    • Effectiveness of one tube osmotic fragility screening in detecting β-thalassemia trait
    • Kattamis C, Efremov G, Pootrakul S. Effectiveness of one tube osmotic fragility screening in detecting β-thalassemia trait. J Met Genet 1981; 18: 266-70.
    • (1981) J Met Genet , vol.18 , pp. 266-270
    • Kattamis, C.1    Efremov, G.2    Pootrakul, S.3
  • 63
    • 0020044813 scopus 로고
    • A screening test for assessing iron status
    • Pintar J, Skikne BS, Cook JD. A screening test for assessing iron status. Blood 1982; 59: 110-3.
    • (1982) Blood , vol.59 , pp. 110-113
    • Pintar, J.1    Skikne, B.S.2    Cook, J.D.3
  • 64
    • 2642525357 scopus 로고    scopus 로고
    • A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia
    • Fucharoen G, Sanchaisuriya K, Sae-Ung N, Dangwibul S, Fucharoen S. A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia. Bull World Health Organ 2004; 82: 364-72.
    • (2004) Bull World Health Organ , vol.82 , pp. 364-372
    • Fucharoen, G.1    Sanchaisuriya, K.2    Sae-Ung, N.3    Dangwibul, S.4    Fucharoen, S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.