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Test ID: SCADZ    
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Full Gene Analysis

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Useful For Suggests clinical disorders or settings where the test may be helpful

Preferred molecular analysis to confirm a diagnosis of short-chain acyl-CoA dehydrogenase deficiency (as a follow-up to the biochemical analyses only)

Testing Algorithm Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

See Newborn Screening Follow-up for Isolated C4 Acylcarnitine Elevations (also applies to any plasma or serum C4 acylcarnitine elevation) in Special Instructions.

Special Instructions Library of PDFs including pertinent information and forms related to the test

Method Name A short description of the method used to perform the test

Polymerase Chain Reaction (PCR)/DNA Sequence Analysis

NY State Available Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Reporting Name Lists a shorter or abbreviated version of the Published Name for a test

SCAD Deficiency, Full Gene Analysis

Aliases Lists additional common names for a test, as an aid in searching

ACADS
SCAD (Short-Chain Acyl-CoA Dehydrogenase) Deficiency
SCADM
Short-Chain Acyl-CoA Dehydrogenase (SCAD)