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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 2
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Short Communication

Prevalence of Hb S (HHB: c.20A > T) in a Honduran Population of African Descent

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Pages 134-137 | Received 30 Jul 2014, Accepted 26 Sep 2014, Published online: 24 Feb 2015

References

  • Williams TN, Weatherall DJ. World distribution, population genetics, and health burden of the hemoglobinopathies. Cold Spring Harb Perspect Med. 2012;2(9):a011692. doi: 10.1101/cshperspect.a011692
  • Aygun B, Odame I. A global perspective on sickle cell disease. Pediatr Blood Cancer. 2012;59(2):386–390. doi: 10.1002/pbc.24175
  • Brown AK, Sleeper LA, Miller ST, et al. Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease. Arch Pediatr Adolesc Med. 1994;148(8):796–804
  • Steinberg MH. Sickle cell anemia, the first molecular disease: Overview of molecular etiology, pathophysiology, and therapeutic approaches. ScientificWorldJournal 2008;8:1295–1324. doi: 10.1100/tsw.2008.157
  • Faúndez A, Meléndez E. Pueblos afrodescendientes de Honduras. Secretaría de Desarrollo de los Pueblos Indígenas y Afrohondureños CMdA, Ed., Proceedings of the meeting held at La Ceiba, Honduras, 18–21 August 2011. 2011:1–52. (Available at http://www.inclusionyequidad.org/sites/default/files/INFORME%20CUMBRE%20FINA.pdf
  • Health in the Americas: Honduras Volume. Pan American Health Organization, 2012. http://www.paho.org/saludenlasamericas/index.php?option=com_content&view=article&id=43&Itemid=50&lang=es
  • Larrañaga N, Mejia RE, Hormaza JI, et al. Genetic structure of Plasmodium falciparum populations across the Honduras-Nicaragua border. Malar J. 2013;12:354. doi: 10.1186/1475-2875-12-354
  • Organización Mundial de la Salud. Concentraciones de hemoglobina para diagnosticar la anemia y evaluar su gravedad. Ginebra: (WHO/NMH/NHD/MNM/11.1), 2011
  • World Health Organization, United Nations University. Iron deficiency anaemia: Assessment, prevention and control, a guide for programme managers. Geneva, Switzerland: World Health Organization, 2001. http://www.who.int/nutrition/publications/en/ida_assessment_prevention_control.pdf
  • de Lamballerie X, Zandotti C, Vignoli C, et al. A one-step microbial DNA extraction method using “Chelex 100” suitable for gene amplification. Res Microbiol. 1992;143(8):785–790
  • Saiki RK, Scharf S, Faloona F, et al. Enzymatic amplification of β-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science. 1985;230(4732):1350–1354
  • Chang JC, Kan YW. Antenatal diagnosis of sickle cell anaemia by direct analysis of the sickle mutation. Lancet. 1981;2(8256):1127–1129
  • Novack V, Finestone AS, Constantini N, et al. The prevalence of low hemoglobin values among new infantry recruits and nonlinear relationship between hemoglobin concentration and physical fitness. Am J Hematol. 2007;82(2):128–133
  • Belisario AR, Rodrigues CV, Martins ML, et al. Coinheritance of α-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia. Hemoglobin. 2010;34(6):516–529
  • Modell B, Darlison M. Global epidemiology of haemoglobin disorders and derived service indicators. Bull World Health Organ. 2008;86(6):480–487
  • World Health Organization. Management of Birth Defects and Haemoglobin Disorders. Report of a Joint WHO-March of Dimes Meeting. Geneva, Switzerland: WHO. 2006; 17–19. May 2006
  • Weatherall D, Akinyanju O, Fucharoen S, et al. Inherited disorders of hemoglobin. In: Jamison DT, Breman JG, Measham AR, et al, Eds. Disease Control Priorities in Developing Countries, 2nd ed. Washington, DC: World Bank. 2006:663–680. ISBN-10: 0-8213-6179-1. Available at http://www.ncbi.nih.gov.books/NBK11728
  • Sáenz GF, Gutiérrez A, Brilla E, et al. Abnormal hemoglobins among Costa Rican negroid population (Spanish). Rev Biol Trop. 1971;19(1):251–256
  • Granda H, Gispert S, Dorticos A, et al. Cuban programme for prevention of sickle cell disease. Lancet. 1991;337(8734):152–153
  • Aguila JD, Zamora MC, Fernandez OA, et al. Comprehensive care for patients with sickle cell disease in Cuba. Haematologica. 2008;93(1):e20. doi: 10.3324/haematol.11986
  • Ferreira TD, Freire AS, Silveira-Lacerda Ede P, et al. A model of genetic guidance for hemoglobinopathy patients and laboratory diagnosis of family members as educational and preventive measures. Rev Bras Hematol Hemoter. 2012;34(5):339–344
  • Fernandes AP, Januario JN, Cangussu CB, et al. Mortality of children with sickle cell disease: A population study. J Pediatr (Rio J). 2010;86(4):279–284
  • Lervolino LG, Baldin PE, Picado SM, et al. Prevalence of sickle cell disease and sickle cell trait in national neonatal screening studies. Rev Bras Hematol Hemoter. 2011;33(1):49–54
  • Feizal J, Miller EI, Gatitido FI, Peña A. Frecuencia de la Hemoglobinopatía “S” en una muestra de población de la raza negra en Trujillo, Colón. Rev Méd Hondur. 1992;60(4):155–159
  • Makani J, Cox SE, Soka D, et al. Mortality in sickle cell anemia in Africa: A prospective cohort study in Tanzania. PLoS One. 2011;6(2):e14699. doi: 10.1371/journal.pone.0014699
  • McGann PT. Sickle cell anemia: An underappreciated and unaddressed contributor to global childhood mortality. J Pediatr. 2014;165(1):18–22
  • World Health Organization. Executive Board, 118th session: Resolutions and Decisions, 2006. Geneva, Switzerland, 2006

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