Guidance

Baby at risk of having sickle cell disease: description in brief

Information to help healthcare professionals speak with parents at risk of having a child with sickle cell disease.

Documents

Details

This publication explains the risks of a baby having sickle cell disease when both parents carry an unusual haemoglobin gene, at least one of which is sickle cell.

It includes information about:

  • what sickle cell disease is
  • the different conditions the baby might inherit
  • diagnostic testing for sickle cell
  • treatment options
  • having another baby

Contact the Screening helpdesk with any queries about this publication, making sure you include its full title.

Updates to this page

Published 1 January 2014
Last updated 12 January 2021 + show all updates
  1. Updated information and reformatted as HTML publication

  2. Updated with new statement on use of personal data and copyright.

  3. Updated version of leaflet.

  4. First published.

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