Surveillance for sickle cell disease, United Republic of Tanzania

Author:

Ambrose Emmanuela E1,Smart Luke R2,Charles Mwesige3,Hernandez Arielle G2,Latham Teresa2,Hokororo Adolfine1,Beyanga Medard3,Howard Thad A2,Kamugisha Erasmus4,McElhinney Kathryn E2,Tebuka Erius5,Ware Russell E2

Affiliation:

1. Department of Paediatrics and Child Health, Catholic University of Health and Allied Sciences, Mwanza, United Republic of Tanzania.

2. Division of Hematology, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati Children’s Hospital, 3333 Burnet Avenue, MLC 7015 Cincinnati, Ohio 45229, United States of America.

3. Department of Laboratory Services, Bugando Medical Centre, Mwanza, United Republic of Tanzania.

4. Department of Biochemistry and Molecular Biology, Catholic University of Health and Allied Sciences, Mwanza, United Republic of Tanzania.

5. Department of Pathology, Catholic University of Health and Allied Sciences, Mwanza, United Republic of Tanzania.

Publisher

WHO Press

Subject

Public Health, Environmental and Occupational Health

Reference52 articles.

1. Sickle cell disease.;Ware;Lancet,2017

2. Sickle cell anemia: an underappreciated and unaddressed contributor to global childhood mortality.;McGann;J Pediatr,2014

3. Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions.;Piel;PLoS Med,2013

4. The distribution of haemoglobin C and its prevalence in newborns in Africa.;Piel;Sci Rep,2013

5. Sickle-cell disease: a strategy for the WHO African region. Report AFR/RC60/8. Geneva: World Health Organization; 2010. Available from: https://www.afro.who.int/sites/default/files/2017-06/afr_rc60_8.pdf [cited 2020 Sep 02].

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