S hemoglobin haplotypes: Their epidemiologic, anthropologic, and clinical significance;Haplotipos de la hemoglobina S: Importancia epidemiologica, antropologica y clinica

Revista Panamericana de Salud Publica/Pan American Journal of Public Health

Volumn 3, Issue 1, 1998, Pages 1-8

  Rodríguez Romero, Walter E ^a   Sáenz Renauld, Germán F ^a   Chaves Villalobos, Mario A ^a  

^a UNIVERSIDAD DE COSTA RICA   (Costa Rica)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN C; HEMOGLOBIN S;

ARTICLE; DNA POLYMORPHISM; ETHNIC GROUP; GENE CLUSTER; GENETIC MARKER; GENOTYPE; HAPLOTYPE; HEMOGLOBINOPATHY; HUMAN; MAJOR CLINICAL STUDY; POPULATION GENETICS; PROGNOSIS; SICKLE CELL ANEMIA;

EID: 0009680930     PISSN: 10204989     EISSN: None     Source Type: Journal    
DOI: 10.1590/S1020-49891998000100001     Document Type: Article

References (46)

1. Wainscoat JS. The haemoglobinopathies. En: Hoffbrand AV, Lewis SM. Postgraduate haematology, 3a ed. London: Heinman Medical Books; 1989:121-144.
2. Rodgers GP, Schetcher AN. Molecular pathology of the hemoglobin structure. En: Hoffman R, Benz E, Shattil S, Fume B, Cohen H. Haematology: basic principles and practice. New York: Churchill-Livingstone; 1991:441-470.
3. Steimberg MH. DNA diagnosis for the detection of sickle hemoglobinopathies. Am J Hematol 1993;43:110-115.
4. Zhang YH, McCabe L, Wilborn M, Therrell B, McCabe ER. Application of molecular genetics in public health: improved follow-up in a neonatal hemoglobinopathy screening program. Biochem Med Metab Biol 1994;52: 27-35.
5. Nieves MA, López MA, De Pablos, JM Garrido F. La reacción en cadena de la polimerasa: aplkación al estudio de la patología del gen β de globina. Biol Clin Hematol 1990;12:121-126.
6. Nagel RL, Ranney HM. Genetic epidemiology of structural mutations of the β gene. Semin Hematol 1990;27:324-359.
7. Nagel RL. Severity, pathobiology, epistatic effects, and genetic markers in sickle cell anemia. Semin Haematol 1991;28:180-201.
8. Adekile AD. Factors associated with the distribution and severity of sickle cell disease in Africa. Sphere 1994;17:1-5.
9. Polimorfismos del ADN. En: Colombo B, Svarch E, Martínez G. Genética y clínica de las hemoglobinas humanas. La Habana: Pueblo y Educación; 1993.
10. Kan YW, Dozy AM. Evolution of the hemoglobin S and C genes in world populations. Science 1980 09:388-391.
11. s-genecluster haplotypes as prognostic indicators of vital organ failure. Semin Hematol 1991;28: 202-208.
12. Schroeder WA, Munger ES, Powars DR. Sickle cell anemia, genetic variations and the trade to the United States. J African History 1990;31:163-180.
13. Fullerton SM, Harding RM, Boyce AJ, Cleggs JB. Molecular and population genetic analysis of allelic sequence diversity at the human β globin locus. Proc Nat Acad Sci USA 1994;91: 1805-1809.
14. Flint J, Harding R, Clegg J, Boyce A. Why are some genetic diseases common? Human Genet 1993;91:101-117.
15. Nagel RL. Sickle cell anemia is a multigene disease. Amer J Hematol 1993;42:96-101.
16. Chelboune Y, Pagnier J, Trabuchet G. Structural analysis of the 5′ flanking region of the β-globin gene in African sickle cell anemia patients: further evidence for three origins of the sickle mutation in Africa. Proc Nat Acad Sci USA. 1988;85:4431-4435.
17. The geographical distribution of the common abnormal Hb variants. En: Lehman H, Huntsman RG. Man's haemoglobins, 2a ed. Philadelphia: JB Lippincott; 1974:301-310.
18. Fischman J. Putting our oldest ancestors in their proper place. Science 1994;265:2011.
19. g: origin, evolution, and aftermath. Blood 1991;78:2165-2172.
20. Livingstone FB. Anthropological aspects of the distributions of the human hemoglobin variants. En: Winter WP, ed. Hemoglobin variants in human populations. Boca Raton, Florida: CRC Press; 1986:17-28.
21. E globin gene. Am J Hum Genet 1984;36:212-217.
22. E gene in Southeast Asia. Proc Nat Acad Sci (USA) 1982;79:608-615.
23. c gene in blacks. Am J Hum Genet 1985; 37:771.
24. Lapoumeroulie C, Dunda O, Trabuchet G, Mony M, Bodo JM, Carnevale P, et al. A novel sickle cell gene of yet another origin in Africa: the Cameroon type. Hum Genet 1992;89: 333-337.
25. s-gene flow from West Africa to North Africa, the Mediterranean, and Southern Europe. Hemoglobin 1992;16:105-112.
26. Auloch JR, Kiline Y, Aksoy M, Yuregir GT, Bakiouglu T, Kutlar A, Kutlar F, Huisman THJ. Sickle cell anemia among Eti-turks. Br J Haematol 1986;64:45-55.
27. Miller B, Olivier N, Salameh M, Ahmed M, Antognetti G, Huisman THJ. Molecular analysis of the high hemoglobin-F phenotype in Saudi-Arabian with sickle cell anemia. N Engl J Med 1987;316:244-256.
28. Pagnier J, Mears JG, Dunda O, Schaeffer-Rego K, Beldjord C, Nagel RL, et al. Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa. Proc Nat Acad Sci (USA) 1984;81:1170-1773.
29. s chromosome with the same haplotype. Am J Hematol 1985;20:297-300.
30. Wainscoat JS, Thein SL, Higgs DR. A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease? Br J Haematol 1985;60:261-268.
31. El-Mouzan M, Al Awang B, Al Torki M. Clinical features of sickle cell disease in eastern Saudi Arab children. Am J Ped Hematol Oncol 1990;12:51-55.
32. s mutation and the unicentric origin of tribal populations in India. Hum Biol 1989;61:479-491.
33. Sáenz GF. Hemoglobinopatías en los países de la Cuenca del Caribe. Rev Biol Trop 1988; 36:361-372.
34. Sáenz GF, Chaves MA, Quintana E. Las hemoglobinopatías en Costa Rica: aspectos históricos, culturales y epidemiológicos. Rev Costarricense Cien Med 1989;7:95-106.
35. s-gene cluster haplotypes. Rev Invest Clin 1994;April(supl):245.
36. s globin gene in blacks: the contribution of recurrent mutation or gene conversion or both. Proc Nat Acad Sci (USA) 1984;81:853-856.
37. Powars D, Chan L, Schroeder WA. The variable expression of sickle cell disease is genetically determined. Sem Hematol 1990;27: 360-370.
38. Mears JG, Lachman HM, Labie D. α thalassemia is related to prolonged survival in sickle cell anemia. Blood 1983;68:286-290.
39. Embury SH, Clark MR, Monroy G, Mohandas N. Concurrent sickle cell anemia and α- thalassemia: effect on pathological properties of sickle erythrocytes. J Clin Invest 1984;73: 116-123.
40. Owang PJ, Ogada T, Beris P, Hattori Y, Lanclor KD. Haplotypes and α globin gene analyses in sickle cell anaemia in patients from Kenya. Br J Haematol 1987;65:211-215.
41. Rodgers GP, Dover G, Uyesaka N, Nboguchi C, Schetcher A, Nienhus A. Augmentation of erythropoietin of the fetal hemoglobin response to hydroxyurea in sickle cell disease. N Engl J Med 1993;328:73-80.
42. Schroeder WA, Powars DR, Kay L. β cluster haplotypes, α gene status and hematological data from SS, SC and S/β thai patients in southern California. Hemoglobin 1989;13: 325-353.
43. Steimberg MH. The interaction of α thalassemia with hemoglobinopathies. Hematol Oncol Clin N Am 1991;5:453-467.
44. Sáenz GF, Chaves M, Rodríguez W, Sánchez G, Barrantes A, Barrenechea M, et al. Frecuencia de β tal y otras hemoglobinopatías en población costarricense de raza negra. Rev Costarricense Cien Med 1990;11:3-10.
45. s-gene-cluster haplotypes in sickle cell anemia. Hematol Oncol Clin N Am 1991;5:475-493.
46. Powars D, Chan L, Schroeder WA. The variable expression of sickle cell disease is genetically determined. Hematol Oncol Clin N Amer 1990;27:360-370.