A5080778672- Hemoglobinopathies and Related Disorders
- Iron Metabolism and Disorders
- Blood groups and transfusion
- Hepatitis B Virus Studies
- Hematological disorders and diagnostics
- Blood disorders and treatments
- Folate and B Vitamins Research
- Chronic Kidney Disease and Diabetes
- Global Maternal and Child Health
- Neutropenia and Cancer Infections
- Epigenetics and DNA Methylation
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Plant Pathogens and Fungal Diseases
- Epilepsy research and treatment
- Fungal Infections and Studies
- Antibiotic Use and Resistance
- Diabetes, Cardiovascular Risks, and Lipoproteins
- Antifungal resistance and susceptibility
- Acute Kidney Injury Research
- Hepatitis C virus research
- Liver Disease Diagnosis and Treatment
- Blood properties and coagulation
- Erythrocyte Function and Pathophysiology
- Liver Disease and Transplantation
- Dialysis and Renal Disease Management
Centre Pasteur du Cameroun
2013-2024
Summary Growth failure ( GF ) in children with sickle cell disease SCD tends to decline high‐income countries, but data are lacking sub‐Saharan Africa. We performed a cross‐sectional study nested the CADRE (Cœur, Artères et DRE panocytose) cohort Mali, Senegal, Cameroon, Gabon and Ivory Coast. patients healthy controls aged 5–21 years old were recruited n = 2583). Frequency of , defined as height, weight or body mass index below 5th percentile on World health Organization growth charts, was...
Haematological values derived from local populations are useful in laboratories to improve diagnoses for patients. In Cameroon, these data not yet available. Moreover, there is great variation baseline parameters pertaining full blood cell count among medical laboratories.This study aimed determine the complete of a healthy adult Cameroonian population use locally ranges our laboratories.A cross-sectional was conducted donors attending three banks Yaoundé November 2015 September 2016. We...
Renal dysfunctions are associated with increased morbidity and mortality in sickle cell disease (SCD). Early detection subsequent management of SCD patients at risk for renal failure essential, however, predictors that can identify developing dysfunction not fully understood. In this study, we have investigated the association 31 known kidney dysfunctions-related variants detected African Americans from multi-ethnic genome wide studies (GWAS) meta-analysis, to kidney-dysfunctions a group 413...
Summary The degree of anaemia in sickle cell disease (SCD) is a well‐known contributor to morbidity and mortality. We aimed explore the factors affecting haemoglobin (Hb) level African SCD patients, considering haemolysis biomarkers (LDH bilirubin level, reticulocyte count), leucocyte platelet counts socio‐demographic characteristics (gender, age group, country residence BMI). research was part CADRE multinational cohort involved 3699 patients living Mali, Senegal, Ivory Coast, Democratic...
Topic: 26. Sickle cell disease Background: (SCD) is one of the most frequent monogenic worldwide leading to production abnormal haemoglobin (Hb) S that causes chronic peripheral haemolysis. Anaemia has been identified as a morbidity and mortality factor SCD in several studies, both developed undeveloped countries, but few studies have analysed determinants Hb level African context. Aims: The aim this study was analyse factors associated with patients SCD, especially disease-specific such...