Form

MCADD: request for extended mutation screen

This form is to request medium-chain acyl-CoA dehydrogenase deficiency (MCADD) investigation of a presumed positive screening case.

This publication was withdrawn on

See current MCADD publications in the NHS newborn blood spot screening programme collection.

Documents

Medium-chain acyl-CoA dehydrogenase deficiency: investigation of presumptive positive screening cases

This file may not be suitable for users of assistive technology. 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 publications@phe.gov.uk. Please tell us what format you need. It will help us if you say what assistive technology you use.

Details

Extended mutation screen for medium-chain acyl-CoA dehydrogenase deficiency (MCADD) after initial screen is positive.

Published 1 December 2010