Premarital genetic screening and care of Tanzanian children with sickle cell disease: a qualitative study on parents’ views and experiences

Author:

Kisanga Esther,Mutagonda Ritah,Myemba David T.,Njiro Belinda J.,Simon Franklin,Marealle Alphonce I.,Mikomangwa Wigilya P.,Kilonzi Manase,Sambayi Godfrey,Bwire George M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Public Health, Environmental and Occupational Health,Epidemiology

Reference16 articles.

1. Ali RMA, Razeq NMA (2017) The lived experience of parents of children with sickle cell disease: a qualitative study. Open J Nurs 07(11):1348–1364

2. World Health Organization. Control of Genetic Diseases (2005) https://www.apps.who.int/gb/archive/pdf_files/EB116/B116_3-en.pdf. Accessed 19 July 2021

3. Bozkurt G (2007) Results from the North Cyprus Thalassemia Prevention Program. Hemoglobin 31(2):257–264

4. Brousse V, Makani J, Rees DC (2014) Management of sickle cell disease in the community. BMJ 348(March):1–9

5. Colorafi KJ, Evans B (2016) Qualitative descriptive methods in health science research. Heal Environ Res Des J 9(4):16–25

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