MCADZ - Overview: Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency Full Gene Analysis

Test Catalog

Test Name

Test ID: MCADZ    
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency Full Gene Analysis

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

Confirmation of diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency (as a follow-up to biochemical analyses)

 

Screening of at-risk carriers of MCAD deficiency when an affected relative has not had molecular testing

 

Diagnosis of MCAD deficiency in autopsy specimens

Reflex Tests Lists test(s) that may or may not be performed, at an additional charge, depending on the result and interpretation of the initial test(s)

Test IDReporting NameAvailable SeparatelyAlways Performed
CULFBFibroblast Culture for Genetic TestYesNo

Testing Algorithm Delineates situation(s) when tests are added to the initial order. This includes reflex and additional tests.

If skin biopsy is received, fibroblast culture for genetic test will be added and charged separately.

 

See Newborn Screening Follow-up for Elevations of C8, C6, and C10 Acylcarnitines (also applies to any plasma or serum C8, C6, and C10 acylcarnitine elevations) in Special Instructions.

Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test

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

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

Yes

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

MCAD Deficiency, Full Gene Analysis

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

985A>G
ACADM
K304E
MCAD Gene Sequence Analysis
MCADS