Literature DB >> 12915349

[Good practices for the study of hemoglobin].

J Bardakdjian-Michau1, J-L Dhondt, R Ducrocq, F Galactéros, A Guyard, F-X Huchet, A Lahary, D Lena-Russo, P Maboudou, M-L North, C Prehu, A-M Soummer, M Verschelde, H Wajcman.   

Abstract

Hemoglobinopathies have become a significant national health problem in France. The biologists have a pivotal role in the genetic diagnoses. Although sickle cell disease (SCD) is the most frequent abnormality found: not less than 200 new cases are observed each year at birth, many other globin gene variations are found in the various ethnic groups. Since 1995 a neonatal sickle cell screening program has been established for at risk newborns. This programme is supported by the "Association française de dépistage et prévention des handicaps de l'enfant" (AFDPHE). The characterization of hemoglobin genetic variations requires a comprehensive set of laboratory techniques for which we specify here main clinical and technical recommendations.

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Year:  2003        PMID: 12915349

Source DB:  PubMed          Journal:  Ann Biol Clin (Paris)        ISSN: 0003-3898            Impact factor:   0.459


  2 in total

1.  DNA testing for sickle cell anemia in Africa: Implementation choices for the Democratic Republic of Congo.

Authors:  Mamy Ngole; Valerie Race; Gloire Mbayabo; Paul Lumbala; Cathy Songo; Prosper Tshilobo Lukusa; Koenraad Devriendt; Gert Matthijs; Aimé Lumaka
Journal:  J Clin Lab Anal       Date:  2022-04-11       Impact factor: 3.124

2.  Unexpected discovery of hemoglobinopathy C/β° thalassemia.

Authors:  Wafaa Bouyarmane; Jean Uwingabiye; Asmaa Biaz; Achraf Rachid; Youness Mechal; Abdellah Dami; Sanae Bouhsain; Zhor Ouzzif; Samira El Machtani Idrissi
Journal:  Clin Case Rep       Date:  2018-09-21
  2 in total

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