Clinical manifestations of sickle cell disease in Africa and its association with foetal haemoglobin parameters
This work highlights important differences and similarities across SCD populations in the three countries. This is important especially in development of interventions in the light of personalised medicine.
Authors
- Florence Urio (ORCID: https://orcid.org/0000-0002-3241-9768)
- Evans Xorse Amuzu (ORCID: https://orcid.org/0000-0001-5977-5706)
- Suraj Yawnumah Abubakar
- Chinedu Okeke
- Emmanuel Balandya (ORCID: https://orcid.org/0000-0002-3707-9985)
- Elliot Eli Dogbe
- Vivian Paintsil (ORCID: https://orcid.org/0000-0002-8965-0549)
- Olasinbo Olumuyiwa Balogun (ORCID: https://orcid.org/0000-0001-9411-2983)
- Petronilla J. Ozumba (ORCID: https://orcid.org/0000-0001-8243-9647)
- Ponsian Peter
- Daniel Ansong (ORCID: https://orcid.org/0000-0003-1328-9117)
- Siana Watoky Nkya (ORCID: https://orcid.org/0000-0001-7576-6279)
- Alex Osei‐Akoto (ORCID: https://orcid.org/0000-0002-6764-4383)
- Julie Makani (ORCID: https://orcid.org/0000-0002-4801-6250)
- Obiageli Nnodu
- Madu Anazoeze
Institutions
- University of Nigeria (NG)
- Muhimbili University of Health and Allied Sciences (TZ)
- Komfo Anokye Teaching Hospital (GH)
- Kwame Nkrumah University of Science and Technology (GH)
- Institute of Human Virology (NG)
- University of Abuja (NG)
Publication Details
- Journal
- Communications Medicine
- Published
- 2025-06-18
- DOI
- https://doi.org/10.1038/s43856-025-00954-z
- Citations
- 5
- Primary Topic
- Hemoglobinopathies and Related Disorders
- Type
- article
- Field-Weighted Citation Impact
- 8.13
Funders
- International Centre for Genetic Engineering and Biotechnology