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.

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


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

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

Published 1 December 2010