ArticleThe Pan African medical journal2017
[Epidemiological, clinical and hematological profiles of homozygous sickle cell disease during the intercritical period among children in Ziguinchor, Senegal].
Article in The Pan African medical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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8 citing papers in PubMed, 27 citations in OpenAlex.
- Prevalence and clinical correlates of splenomegaly in sickle cell disease patients: An observational study in Western India.Medical journal, Armed Forces India · 2025Article
- Epidemiological and clinical characteristics of 66 Tunisian Sickle cell syndrome patients.African health sciences · 2023Article
- Clinical profile of sickle cell disease in children treated at "Cliniques Universitaires de Bukavu" and "Clinique Ami des Enfants", Bukavu, Democratic Republic of the Congo.The Pan African medical journal · 2022Article
- [Platelet count in the steady state phase and clinical severity of sickle cell disease in a reference centre for sickle cell disease in Mali].The Pan African medical journal · 2022Article
- Hybridized ZoonoticMicroorganisms · 2021Article
- Improvement of SCD morbimortality in children: experience in a remote area of an African country.BMC health services research · 2021Article
- Sickle Cell Disease in the Democratic Republic of Congo: Assessing Physicians' Knowledge and Practices.Tropical medicine and infectious disease · 2020Article
- Sickle Cell Disease in Mauritania: epidemiological, clinical and therapeutic aspects about 135 cases.La Tunisie medicaleArticle
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Authors and funding
13 authors at 6 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sickle cell disease poses a public health problem in Senegal. It mainly affects children and adolescents. This study aimed to determine the epidemiological, clinical and hematological profiles of homozygous (SS) sickle cell disease in a cohort of children followed-up at the Peace Hospital in Ziguinchor. We conducted a retrospective study of the medical records from children with sickle cell disease. All patients aged between 2 months and 21 years with sickle cell disease SS during the intercritical period, hospitalized during the study period from 1
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