Related Experiment Video
Updated: Nov 5, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
[Newborn screening for sickle cell disease in France]
Valentine Brousse1, Bichr Allaf2, Malika Benkerrou3
1Centre de référence de la drépanocytose, Hôpital universitaire Robert Debré, 48 boulevard Sérurier, AP-HP, 75019 Paris, France - Inserm UMRS1134 - Biologie intégrée du globule rouge, 6 rue Alexandre-Cabanel, 75015 Paris, France.
Abstract:
Newborn screening (NBS) for sickle cell disease (SCD) in France has allowed the identification of 9,260 children with SCD since 1989, including 583 in 2019. In mainland France, however, SCD screening is targeted to newborns identified at risk of SCD, i.e born from parents originating from countries with a high SCD prevalence. This screening program, combined to prophylactic measures and a well-organized social and health network in France, has demonstrated considerable efficacy in reducing childhood mortality as well as severe infectious, anemic and neurovascular complications in childhood. SCD NBS has additionally allowed the identification of 180,687 heterozygous (AS) children since 1989. The increasing incidence of SCD (1/1,303 new-borns identified in 2019 versus 1/2,089 in 2009) now pleads for universal NBS and strong advocacy regarding SCD, the most frequent disease identified by NBS in France, and a major public health issue.

