Beliefs negatively mediate adolescents’ and adults’ knowledge about sickle cell disease prevention and relationship choices; a one-center exploratory study in Central Region, Ghana

Author:

Laar Godfred Kiteinkwa,Mwinbeku Justine,Pappoe Ebenezer Allotey,Obike Emmanuella,Ankomah Elizabeth,Baidoo Belinda,Morrison Diana Baaba,Boachie Joseph,Adu Patrick

Publisher

Springer Science and Business Media LLC

Reference31 articles.

1. Assembly UNG. Recognition of sickle-cell anaemia as a public health problem: draft resolution / Angola, Austria, Belgium, Benin, Brazil, Cameroon, Cape Verde, Central African Republic, Comoros, Congo, Côte d’Ivoire, Democratic Republic of the Congo, Djibouti, France, Gabon, Ghana, Monaco, Senegal, Togo and Zambia. In: Assembly G, editor. 2008. A/RES/63/237. Available at: https://digitallibrary.un.org/record/644129?v=pdf.

2. Asare EV, Wilson I, Benneh-Akwasi Kuma AA, Dei-Adomakoh Y, Sey F, Olayemi E. Burden of sickle cell disease in Ghana: the Korle-Bu experience. Adv Hematol. 2018;2018:6161270.

3. Ohene-Frempong K, Oduro J, Tetteh H, Nkrumah FJP. Screening newborns for sickle cell disease in Ghana. Pediatrics. 2008;121(Supplement_2):S120–1.

4. Kyerewaa Edwin A, Edwin F, Etwire V. Controlling sickle cell disease in Ghana–ethics and options. Pan Afr Med J. 2011;10:14.

5. Oyewo A, Salubi-Udu J, Khalaf Y, Braude P, Renwick P, Lashwood A, El-Toukhy T, Oteng-Ntim E. Preimplantation genetic diagnosis for the prevention of sickle cell disease: current trends and barriers to uptake in a London teaching hospital. Hum Fertil. 2009;12(3):153–9.

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