Ontology highlight
ABSTRACT:
SUBMITTER: Tossea SK
PROVIDER: S-EPMC5880027 | biostudies-literature | 2018 Apr
REPOSITORIES: biostudies-literature
Tossea Stephane Koui SK Adji Eric Gbessi EG Coulibaly Baba B Ako Berenger Ako BA Coulibaly David Ngolo DN Joly Philippe P Assi Serge-Brice SB Toure Andre A Jambou Ronan R
BMC research notes 20180402 1
<h4>Objectives</h4>Sickle cell anemia is due to a mutations on the betaglobin gene, inducing abnormal hemoglobin. In West Africa the main mutations lead to S or C types of hemoglobin. Patients with homozygote mutations seem protected against severe malaria, but not against mild disease. The prevalence of abnormal hemoglobin among patients attending dispensaries for mild malaria is thus unknown. A retrospective study was conducted to update data on the prevalence of S and C hemoglobin among patie ...[more]