Literature DB >> 3774535

[Epidemiologic study of hemoglobinopathies in the Congo in 2,257 newborn infants].

M Djembo-Taty, M Tchiloemba, F Galacteros, J Rosa, P Lissouba.   

Abstract

A systematic examination of 2,257 Congolese newborns from Brazzaville for abnormal hemoglobins has been conducted. Gene frequency for HbS was 0.117; no HbC was found. Of the sample 14.4% had detectable amounts of Hb Bart's. Beta-thalassemia trait frequency was approximately estimated to 0.3%, 5 mutations of gamma chain, and 1 mutation for alpha chain were detected.

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Year:  1986        PMID: 3774535

Source DB:  PubMed          Journal:  Nouv Rev Fr Hematol


  4 in total

1.  Hemoglobin variants identified in the Uganda Sickle Surveillance Study.

Authors:  Beverly A Schaefer; Charles Kiyaga; Thad A Howard; Grace Ndeezi; Arielle G Hernandez; Isaac Ssewanyana; Mary C Paniagua; Christopher M Ndugwa; Jane R Aceng; Russell E Ware
Journal:  Blood Adv       Date:  2016-11-22

2.  alpha-Thalassaemia in Tunisia: some epidemiological and molecular data.

Authors:  H Siala; F Ouali; T Messaoud; A Bibi; S Fattoum
Journal:  J Genet       Date:  2008-12       Impact factor: 1.166

3.  Neonatal Screening for Sickle Cell Disease in Congo.

Authors:  Alexis Elira Dokekias; Lethso Thibaut Ocko Gokaba; Josué Simo Louokdom; Lydie Ngolet Ocini; Firmine Olivia Galiba Atipo Tsiba; Coreillia Irène Ondzotto Ibatta; Quentin Ngoma Kouandzi; Serge Talomg Tamekue; Jayne Chelsea Bango; Jade Vanessa Nziengui Mboumba; Simon Charles Kobawila
Journal:  Anemia       Date:  2022-02-03

4.  Routine Screening for Sickle Cell Disease during Pregnancy: Epidemiological and Haemoglobin Profile in Congo.

Authors:  Alexis Elira Dokekias; Josué Simo Louokdom; Letso Thibaut Ocko Gokaba; Firmine Olivia Galiba Atipo Tsiba Gokaba; Jayne Chelsea Bango; Lydie Ngolet Ocini; Clatere Itoua; James Taylor
Journal:  J Neonatal Biol       Date:  2022-03-14
  4 in total

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