Genetic Test Details | Ontario Health

VLCAD deficiency

Test Information

Title: VLCAD deficiency
Lab: Newborn Screening Ontario
Category: Metabolic
Sub Category: Fatty Acid Oxidation Diseases
Gene/Platform/Region List: ACADVL
Test type: Single Gene
Samples Accepted: Blood , DNA , Dried Blood Spot (accepted ONLY for exceptional circumstances)
Indications: Diagnosis , Carrier Cascade Testing
Test Methodology: Sequencing
Disease/Condition: Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency, VLCAD Deficiency

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