Guidance
Baby at risk of having thalassaemia: description in brief
Information to help healthcare professionals speak with parents at risk of having a child with thalassaemia.
Documents
Details
This publication explains the risks for a baby when both parents carry an unusual haemoglobin gene, at least one of which is for thalassaemia.
It includes information about:
- what thalassaemia is
- the different conditions the baby might inherit
- diagnostic testing for thalassaemia
- 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 2014Last updated 12 January 2021 + show all updates
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Updated information for parents and reformatted as HTML publication.
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Updated with new statement on use of personal data and copyright.
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Updated version of patient information leaflet.
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First published.