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.

From:
NHS England
Published
1 November 2010
Last updated
4 April 2025 — See all updates

Applies to England

Documents

MCADD: summary

HTML

MCADD: detailed information

HTML

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.

Updates to this page

Published 1 November 2010
Last updated 4 April 2025 + show all updates

  1. Changed lead organisation to NHS England. Removed reference to screening helpdesk. Removed references to PHE.

  2. 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.

  3. Updated with latest clinical information.

  4. Converted attachment from PDF to HTML.

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

  6. First published.

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