Display Settings:

Format

Send to:

Choose Destination
See comment in PubMed Commons below
J Clin Pathol. 2009 Jan;62(1):31-3. doi: 10.1136/jcp.2008.058867.

Neonatal screening for sickle cell disease in France.

Author information

  • 1Service de Biochimie et de Génétique, Unité Fonctionnelle de Génétique, Centre Hospitalier Universitaire Henri-Mondor (AP-HP), Créteil, France. josiane.michau@hmn.aphp.fr

Erratum in

  • J Clin Pathol. 2009 Sep;62(9):864. Badens, C [added]; Ducrocq, R [added]; Elion, J [added]; Perini, J M [added].

Abstract

BACKGROUND:

As a result of population growth in African-Caribbean regions of overseas France, and now immigration essentially from North and sub-Saharan Africa to mainland France, neonatal screening for sickle cell disease (SCD) has been performed in France since 1985 in Guadalupe and dependencies, as a universal test. After several pilot studies, screening was gradually extended to mainland France in 1996. Since 2000, the test has been performed at national level for all newborns defined as being "at risk" for SCD based on ethnic origin.

METHODS:

A dry blood sample is obtained by heel stick and analysed by isoelectric focusing as a first-line method, followed by either high-performance liquid chromatography or acid agar electrophoresis for confirmation, whenever a variant haemoglobin is observed on isoelectric focusing.

RESULTS:

In 2007, 28.45% of all newborns in mainland France were screened for SCD. Since 1996, a total of 3,890 newborns have been found to have SCD, and they have been followed up by reference paediatricians.

CONCLUSION:

Although screening for SCD at birth in France is not universal, it appears that missed babies are relatively infrequent. Despite obvious sociological problems inherent to the at-risk population, the follow-up of SCD babies is rather successful. Due to the birth prevalence of SCD in France, especially in comparison with other common genetic diseases, screening all newborns regardless of ethnic origin is an issue that is being addressed.

PMID:
19103855
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for HighWire
    Loading ...
    Write to the Help Desk