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.

From:
Public Health England
Published
1 December 2010

This publication was withdrawn on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

MS Word Document, 40 KB

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