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Volumn 3, Issue 5, 2013, Pages

Clinical Manifestations of α-thalassemia

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EID: 84879035265     PISSN: None     EISSN: 21571422     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (51)

References (53)
  • 1
    • 29544440640 scopus 로고    scopus 로고
    • Vascular-type disruptive defects in fetuses with homozygous α-thalassemia: Report of two cases and review of the literature
    • Adam M.P., Chueh J, El-Sayed YY, Stenzel A, Vogel H, Weaver D.D., Hoyme HE. 2005. Vascular-type disruptive defects in fetuses with homozygous α-thalassemia: Report of two cases and review of the literature. Prenat Diagn 25: 1088-1096.
    • (2005) Prenat Diagn , vol.25 , pp. 1088-1096
    • Adam, M.P.1    Chueh, J.2    El-Sayed, Y.Y.3    Stenzel, A.4    Vogel, H.5    Weaver, D.D.6    Hoyme, H.E.7
  • 2
    • 69249157345 scopus 로고    scopus 로고
    • Organ-specific hemosiderosis and functional correlation in Chinese patients with thalassemia intermedia and hemoglobin H disease
    • Au W.Y., Lam WW, Chu WW, Tam S, Wong WK, Lau J, Yeung Y.M., Liu HS, Liang R. 2009. Organ-specific hemosiderosis and functional correlation in Chinese patients with thalassemia intermedia and hemoglobin H disease. Ann Hematol 88: 947-950.
    • (2009) Ann Hematol , vol.88 , pp. 947-950
    • Au, W.Y.1    Lam, W.W.2    Chu, W.W.3    Tam, S.4    Wong, W.K.5    Lau, J.6    Yeung, Y.M.7    Liu, H.S.8    Liang, R.9
  • 3
    • 79951961551 scopus 로고    scopus 로고
    • Newborn screening for α-thalassemia-keepingupwithglobalization
    • Benz EJ Jr. 2011. Newborn screening for α-thalassemia-keepingupwithglobalization. NEngl JMed364:770-771.
    • (2011) NEngl JMed , vol.364 , pp. 770-771
    • Benz Jr., E.J.1
  • 6
    • 33645078392 scopus 로고    scopus 로고
    • Use of the oral chelator deferiprone in the treatment of iron overload in patients with Hb H disease
    • Chan J.C., Chim CS, Ooi CG, Cheung B, Liang R, Chan TK, Chan V. 2006. Use of the oral chelator deferiprone in the treatment of iron overload in patients with Hb H disease. Br J Haematol 133: 198-205.
    • (2006) Br J Haematol , vol.133 , pp. 198-205
    • Chan, J.C.1    Chim, C.S.2    Ooi, C.G.3    Cheung, B.4    Liang, R.5    Chan, T.K.6    Chan, V.7
  • 7
    • 0032055871 scopus 로고    scopus 로고
    • Hydrops fetalis caused by α-thalassemia: An emerging health care problem
    • Chui D.H., Waye JS. 1998. Hydrops fetalis caused by α-thalassemia: An emerging health care problem. Blood 91: 2213-2222.
    • (1998) Blood , vol.91 , pp. 2213-2222
    • Chui, D.H.1    Waye, J.S.2
  • 8
    • 0037305250 scopus 로고    scopus 로고
    • HemoglobinHdisease: Not necessarily a benign disorder
    • ChuiDH, FucharoenS, ChanV. 2003. HemoglobinHdisease: Not necessarily a benign disorder. Blood 101: 791-800.
    • (2003) Blood , vol.101 , pp. 791-800
    • Chui, D.H.1    Fucharoen, S.2    Chan, V.3
  • 11
  • 13
    • 77949445115 scopus 로고    scopus 로고
    • Newborn screening for non-sickling hemoglobinopathies
    • Hoppe CC. 2009. Newborn screening for non-sickling hemoglobinopathies. Hematology Am Soc Hematol Educ Program 19-25.
    • (2009) Hematology Am Soc Hematol Educ Program , pp. 19-25
    • Hoppe, C.C.1
  • 14
    • 77957961389 scopus 로고    scopus 로고
    • Application of an expanded multiplex genotyping assay for the simultaneous detection of Hemoglobin Constant Spring and common deletional α-thalassemia mutations
    • Kidd J.L., Azimi M, Lubin B, Vichinsky E, Hoppe C. 2010. Application of an expanded multiplex genotyping assay for the simultaneous detection of Hemoglobin Constant Spring and common deletional α-thalassemia mutations. Int J Lab Hematol 32: 373-380.
    • (2010) Int J Lab Hematol , vol.32 , pp. 373-380
    • Kidd, J.L.1    Azimi, M.2    Lubin, B.3    Vichinsky, E.4    Hoppe, C.5
  • 16
    • 0036173092 scopus 로고    scopus 로고
    • Middle cerebral artery Doppler study in fetuses with homozygous α-thalassaemia-1 at 12-13 weeks of gestation
    • Lam Y.H., Tang MH. 2002. Middle cerebral artery Doppler study in fetuses with homozygous α-thalassaemia-1 at 12-13 weeks of gestation. Prenat Diagn 22: 56-58.
    • (2002) Prenat Diagn , vol.22 , pp. 56-58
    • Lam, Y.H.1    Tang, M.H.2
  • 17
    • 0030905118 scopus 로고    scopus 로고
    • Prevalence and genotypes of α-and βthalassemia carriers in Hong-implications for population screening
    • Lau Y.L., Chan LC, Chan YY, Ha SY, Yeung CY, Waye JS, Chui DH. 1997. Prevalence and genotypes of α-and βthalassemia carriers in Hong-implications for population screening. N Engl J Med 336: 1298-1301.
    • (1997) N Engl J Med , vol.336 , pp. 1298-1301
    • Lau, Y.L.1    Chan, L.C.2    Chan, Y.Y.3    Ha, S.Y.4    Yeung, C.Y.5    Waye, J.S.6    Chui, D.H.7
  • 18
    • 34447339997 scopus 로고    scopus 로고
    • Outcome of intensive care of homozygous α-thalassaemia without prior intra-uterine therapy
    • Lee S.Y., Chow CB, Li CK, Chiu MC. 2007. Outcome of intensive care of homozygous α-thalassaemia without prior intra-uterine therapy. J Paediatr Child Health 43: 546-550.
    • (2007) J Paediatr Child Health , vol.43 , pp. 546-550
    • Lee, S.Y.1    Chow, C.B.2    Li, C.K.3    Chiu, M.C.4
  • 19
    • 84877135776 scopus 로고    scopus 로고
    • The search for genetic modifiers of disease severity in the β-hemoglobinopathies
    • Lettre G. 2012. The search for genetic modifiers of disease severity in the β-hemoglobinopathies. Cold Spring Harb Perspect Med 2: a015032.
    • (2012) Cold Spring Harb Perspect Med , vol.2
    • Lettre, G.1
  • 20
    • 0036153945 scopus 로고    scopus 로고
    • Serial sonographic findings of four fetuses with homozygous α-thalassemia-1 from 21 weeks onwards
    • Leung W.C., Oepkes D, Seaward G, Ryan G. 2002. Serial sonographic findings of four fetuses with homozygous α-thalassemia-1 from 21 weeks onwards. UltrasoundObstet Gynecol 19: 56-59.
    • (2002) UltrasoundObstet Gynecol , vol.19 , pp. 56-59
    • Leung, W.C.1    Oepkes, D.2    Seaward, G.3    Ryan, G.4
  • 21
    • 33744463110 scopus 로고    scopus 로고
    • Detection of α-thalassemia in β-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening
    • Li D., Liao C, Li J, Xie X, Huang Y, Zhong H. 2006. Detection of α-thalassemia in β-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening. Haematologica 91: 649-651.
    • (2006) Haematologica , vol.91 , pp. 649-651
    • Li, D.1    Liao, C.2    Li, J.3    Xie, X.4    Huang, Y.5    Zhong, H.6
  • 22
    • 0021807743 scopus 로고
    • Homozygous α-thalassaemia: Clinical presentation, diagnosis and management. A reviewof 46 cases
    • Liang S.T., Wong VC, SoWW, Ma HK, Chan V, Todd D. 1985. Homozygous α-thalassaemia: Clinical presentation, diagnosis and management. A reviewof 46 cases. Br JObstet Gynaecol 92: 680-684.
    • (1985) Br JObstet Gynaecol , vol.92 , pp. 680-684
    • Liang, S.T.1    Wong, V.C.2    So, W.W.3    Ma, H.K.4    Chan, V.5    Todd, D.6
  • 23
    • 36248946234 scopus 로고    scopus 로고
    • Prenatal control of Hb Bart's disease in southern China
    • Liao C., Li Q, Wei J, Feng Q, Li J, Huang Y, Li D. 2007. Prenatal control of Hb Bart's disease in southern China. Hemoglobin 31: 471-475.
    • (2007) Hemoglobin , vol.31 , pp. 471-475
    • Liao, C.1    Li, Q.2    Wei, J.3    Feng, Q.4    Li, J.5    Huang, Y.6    Li, D.7
  • 26
    • 27144472774 scopus 로고    scopus 로고
    • Neurodevelopmental outcome and haematological course of a long-time survivor with homozygous α-thalassaemia: Case report and review of the literature
    • Lucke T., Pfister S, Durken M. 2005. Neurodevelopmental outcome and haematological course of a long-time survivor with homozygous α-thalassaemia: Case report and review of the literature. Acta Paediatr 94: 1330-1333.
    • (2005) Acta Paediatr , vol.94 , pp. 1330-1333
    • Lucke, T.1    Pfister, S.2    Durken, M.3
  • 27
    • 0002049948 scopus 로고    scopus 로고
    • Noninvasive diagnosis by Doppler ultrasonography of fetal anemia due to maternal red-cell alloimmunization. Collaborative Group for Doppler Assessment of the Blood Velocity in Anemic Fetuses
    • Mari G., Deter RL, Carpenter RL, Rahman F, Zimmerman R, Moise KJ Jr, Dorman KF, Ludomirsky A, Gonzalez R, Gomez R., et al. 2000. Noninvasive diagnosis by Doppler ultrasonography of fetal anemia due to maternal red-cell alloimmunization. Collaborative Group for Doppler Assessment of the Blood Velocity in Anemic Fetuses. N Engl J Med 342: 9-14.
    • (2000) N Engl J Med , vol.342 , pp. 9-14
    • Mari, G.1    Deter, R.L.2    Carpenter, R.L.3    Rahman, F.4    Zimmerman, R.5    Moise Jr., K.J.6    Dorman, K.F.7    Ludomirsky, A.8    Gonzalez, R.9    Gomez, R.10
  • 29
    • 38549170037 scopus 로고    scopus 로고
    • The usefulness of middle cerebral artery Doppler assessment in the treatment of the fetus at risk for anemia
    • Moise KJ Jr. 2008. The usefulness of middle cerebral artery Doppler assessment in the treatment of the fetus at risk for anemia. Am J Obstet Gynecol 198: e161-e164.
    • (2008) Am J Obstet Gynecol , vol.198
    • Moise Jr., K.J.1
  • 31
    • 54249153275 scopus 로고    scopus 로고
    • Hb Constant Spring [α142, Term → Gln (TAA. CAA in α2)] in the α-thalassemia of anemic patients in Myanmar
    • NeW, Harano K, Harano T, Kyaw-S, Aye-Aye M, Khin T-A, Okada S. 2008. Hb Constant Spring [α142, Term → Gln (TAA. CAA in α2)] in the α-thalassemia of anemic patients in Myanmar. Hemoglobin 32: 454-461.
    • (2008) Hemoglobin , vol.32 , pp. 454-461
    • Ne, W.1    Harano, K.2    Harano, T.3    Kyaw, S.4    Aye-Aye, M.5    Khin, T.-A.6    Okada, S.7
  • 36
    • 34250344619 scopus 로고    scopus 로고
    • Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different α0-thalassemia determinants
    • Siriratmanawong N., Pinmuang-Ngam C, Fucharoen G, Fucharoen S. 2007. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different α0-thalassemia determinants. Fetal Diagn Ther 22: 264-268.
    • (2007) Fetal Diagn Ther , vol.22 , pp. 264-268
    • Siriratmanawong, N.1    Pinmuang-Ngam, C.2    Fucharoen, G.3    Fucharoen, S.4
  • 37
    • 56749130072 scopus 로고    scopus 로고
    • Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at midpregnancy
    • Srisupundit K., PiyamongkolW, Tongsong T. 2008. Comparison of red blood cell hematology among normal, α-thalassemia-1 trait, and hemoglobin Bart's fetuses at midpregnancy. Am J Hematol 83: 908-910.
    • (2008) Am J Hematol , vol.83 , pp. 908-910
    • Srisupundit, K.1    Piyamongkol, W.2    Tongsong, T.3
  • 38
    • 0030956139 scopus 로고    scopus 로고
    • Hemoglobin H-Constant Spring disease: An under recognized, severe form of α thalassemia
    • Styles L., Foote D, Kleman K, Vichinsky E. 1997. Hemoglobin H-Constant Spring disease: An under recognized, severe form of α thalassemia. Int J Pediatr Hematol Oncol 6: 69-74.
    • (1997) Int J Pediatr Hematol Oncol , vol.6 , pp. 69-74
    • Styles, L.1    Foote, D.2    Kleman, K.3    Vichinsky, E.4
  • 40
    • 0020437420 scopus 로고
    • Venous thrombosis in haemoglobin H disease after splenectomy
    • Tso S.C., Chan TK, Todd D. 1982. Venous thrombosis in haemoglobin H disease after splenectomy. Aust NZ J Med 12: 635-638.
    • (1982) Aust NZ J Med , vol.12 , pp. 635-638
    • Tso, S.C.1    Chan, T.K.2    Todd, D.3
  • 41
    • 77949465117 scopus 로고    scopus 로고
    • α Thalassemia major-new mutations, intrauterine management, and outcomes
    • Vichinsky EP. 2009. α Thalassemia major-new mutations, intrauterine management, and outcomes. Hematology Am Soc Hematol Educ Program 35-41.
    • (2009) Hematology Am Soc Hematol Educ Program , pp. 35-41
    • Vichinsky, E.P.1
  • 42
    • 77955914916 scopus 로고    scopus 로고
    • Complexity of α thalassemia: Growing health problem with new approaches to screening, diagnosis, and therapy
    • Vichinsky E. 2010. Complexity of α thalassemia: Growing health problem with new approaches to screening, diagnosis, and therapy. Ann NY Acad Sci 1202: 180-187.
    • (2010) Ann NY Acad Sci , vol.1202 , pp. 180-187
    • Vichinsky, E.1
  • 43
    • 84861397221 scopus 로고    scopus 로고
    • Advances in the treatment of α-thalassemia
    • Vichinsky E. 2012. Advances in the treatment of α-thalassemia. Blood Rev 26: S31-S34.
    • (2012) Blood Rev , vol.26
    • Vichinsky, E.1
  • 44
    • 84877141931 scopus 로고    scopus 로고
    • Successful hematopoietic cell transplantation for α thalassemia major
    • Vichinsky E., Chu J, Walters M, et al. 2010. Successful hematopoietic cell transplantation for α thalassemia major. Pediatr Blood Cancer 54: 840.
    • (2010) Pediatr Blood Cancer , vol.54 , pp. 840
    • Vichinsky, E.1    Chu, J.2    Walters, M.3
  • 45
    • 59249101341 scopus 로고    scopus 로고
    • Hemoglobinopathies worldwide: Present and future
    • Weatherall DJ. 2008. Hemoglobinopathies worldwide: Present and future. Curr Mol Med 8: 592-599.
    • (2008) Curr Mol Med , vol.8 , pp. 592-599
    • Weatherall, D.J.1
  • 48
    • 84879287709 scopus 로고    scopus 로고
    • World distribution, population genetics, and health burden of the hemoglobinopathies
    • Williams T.N., Weatherall DJ. 2012. World distribution, population genetics, and health burden of the hemoglobinopathies. Cold Spring Harbor Perspect Med 2: a11692.
    • (2012) Cold Spring Harbor Perspect Med , vol.2
    • Williams, T.N.1    Weatherall, D.J.2
  • 49
    • 67449095660 scopus 로고    scopus 로고
    • A survey of pregnancies with Hb Bart's disease in Mainland China
    • Yang Y., Li DZ. 2009. A survey of pregnancies with Hb Bart's disease in Mainland China. Hemoglobin 33: 132-136.
    • (2009) Hemoglobin , vol.33 , pp. 132-136
    • Yang, Y.1    Li, D.Z.2
  • 50
    • 64149103412 scopus 로고    scopus 로고
    • Homozygous α-thalassemia treated with intrauterine transfusions and unrelated donor hematopoietic cell transplantation
    • Yi J.S., Moertel CL, Baker KS. 2009. Homozygous α-thalassemia treated with intrauterine transfusions and unrelated donor hematopoietic cell transplantation. J Pediatr 154: 766-768.
    • (2009) J Pediatr , vol.154 , pp. 766-768
    • Yi, J.S.1    Moertel, C.L.2    Baker, K.S.3
  • 51
  • 53
    • 0036634662 scopus 로고    scopus 로고
    • Longitudinal measurement of peak systolic velocity in the fetal middle cerebral artery for monitoring pregnancies complicated by red cell alloimmunisation: A prospective multicentre trial with intention-to-treat
    • Zimmerman R., Carpenter RJ Jr, Durig P, Mari G. 2002. Longitudinal measurement of peak systolic velocity in the fetal middle cerebral artery for monitoring pregnancies complicated by red cell alloimmunisation: A prospective multicentre trial with intention-to-treat. BJOG 109: 746-752.
    • (2002) BJOG , vol.109 , pp. 746-752
    • Zimmerman, R.1    Carpenter Jr., R.J.2    Durig, P.3    Mari, G.4


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