Guidance

MCADD: information for parents

Information and advice for parents of babies with suspected medium-chain acyl-CoA dehydrogenase deficiency (MCADD) following a baby’s screening test result.

Applies to England

Documents

MCADD: summary (for print)

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MCADD: detailed information (for print)

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Details

Information and advice for parents of babies with suspected MCADD 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 November 2010
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 information.

  3. Converted attachment from PDF to HTML.

  4. One of a suite of updated inherited metabolic diseases leaflets.

  5. First published.

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