Neonatal Screening for Sickle Cell Disease in Congo

INTRODUCTION: Sickle cell disease is an autosomal recessive inherited disorder due to the mutation of a gene coding for the globin beta chain. The aim of this study is to update the epidemiological data on hemoglobinoses, in particular sickle cell disease in newborns in Congo. MATERIALS AND METHODS:...

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Detalles Bibliográficos
Autores principales: Dokekias, Alexis Elira, Ocko Gokaba, Lethso Thibaut, Louokdom, Josué Simo, Ocini, Lydie Ngolet, Galiba Atipo Tsiba, Firmine Olivia, Ondzotto Ibatta, Coreillia Irène, Kouandzi, Quentin Ngoma, Tamekue, Serge Talomg, Bango, Jayne Chelsea, Nziengui Mboumba, Jade Vanessa, Kobawila, Simon Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831066/
https://www.ncbi.nlm.nih.gov/pubmed/35154827
http://dx.doi.org/10.1155/2022/9970315

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831066/
https://www.ncbi.nlm.nih.gov/pubmed/35154827
http://dx.doi.org/10.1155/2022/9970315

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