Neugeborenenscreening auf Sichelzellkrankheit in Deutschland

Die Sichelzellkrankheit (SCD) ist eine angeborene Blutkrankheit, die unerkannt mit einer signifikanten Frühmorbidität und -mortalität verbunden ist. Da die Diagnose schon bei Geburt mit einer hohen Zuverlässigkeit gestellt werden kann, hat der Gemeinsame Bundesausschuss (G-BA) die Erweiterung des Neugeborenenscreenings (NBS) um die SCD beschlossen. Es ist zu erwarten, dass die SCD eine der häufigsten Diagnosen im dann 18 Zielkrankheiten umfassenden deutschen NBS-Programm sein wird.

Publikationsverlauf

Artikel online veröffentlicht:
04. November 2021

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