Guidance

Homocystinuria (HCU): information for parents

Information for parents about homocystinuria (HCU) following a baby’s screening test result.

Applies to England

Documents

Homocystinuria (HCU): summary (for print)

Request an accessible format.
If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email [email protected]. Please tell us what format you need. It will help us if you say what assistive technology you use.

Homocystinuria (HCU): detailed information (for print)

Request an accessible format.
If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email [email protected]. Please tell us what format you need. It will help us if you say what assistive technology you use.

Details

Information and advice for parents of babies with suspected HCU following newborn blood spot screening. Healthcare professionals should use it to support them in their conversations with parents.

This information is available in A4 PDF format (in English) to print out and provide for people who cannot access digital information (see list above).

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

Updates to this page

Published 1 August 2013
Last updated 18 November 2021 + show all updates
  1. Combined separate 'overview' and 'further information' leaflets into one publication. Changed 'overview' to 'summary' and 'further information' to 'detailed information'. Addition of plain A4 PDF version for printing, to provide for people unable to access this information online.

  2. Updated with latest clinical guidance.

  3. Converted attachment from PDF to HTML.

  4. One of a suite of revised and updated inherited metabolic disease leaflets.

  5. First published.

Sign up for emails or print this page