Overview of current progress and challenges in diagnosis, and management of pediatric sickle cell disease in Democratic Republic of the Congo-Reference-Cited by-同舟云学术

Overview of current progress and challenges in diagnosis, and management of pediatric sickle cell disease in Democratic Republic of the Congo

Published:2022-01-24 Issue:1 Volume:27 Page:132-140
ISSN:1607-8454
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Kasai Emmanuel Tebandite¹^ORCID,Alworong’a Opara Jean Pierre¹,Ntokamunda Kadima Justin²,Kalenga Masendu³,Batina Agasa Salomon⁴,Marini Djang’eing‘a Roland²⁵,Boemer François⁶

Affiliation:

1. Department of Pediatrics, Faculty of Medicine and Pharmacy, University of Kisangani, Kisangani, Democratic Republic of the Congo

2. Department of Pharmacy, Faculty of Medicine and Pharmacy, University of Kisangani, Kisangani, Democratic Republic of the Congo

3. Department of Pediatrics, Faculty of Medicine, University of Liege, Liege, Beligium

4. Department of Internal Medicine, Faculty of Medicine and Pharmacy, University of Kisangani, Kisangani, Democratic Republic of the Congo

5. Laboratory of Analytical Pharmaceutical Chemistry, Faculty of Medicine, University of Liege, Liege, Belgium

6. Biochemical Genetics Laboratory, Human Genetics, CHU of Liege, University of Liège, Liege, Belgium

Publisher

Informa UK Limited

Subject

Hematology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/16078454.2021.2023399

Reference54 articles.

1. CDC. Hemoglobinopathies: current practices for screening, confirmation and follow-up. APHL. 2015. [Cited 2021 January 12]. Available from: https://www.cdc.gov/ncbddd/sicklecell/documents/nbs_hemoglobinopathy-testing_122015.pdf.

2. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

3. Advances in detection of hemoglobinopathies

4. Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimates

5. The clinical characteristics of Congolese children and adolescents suffering from sickle-cell anemia are marked by the high frequencies of epistaxis compared to Western series

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