Genetic Test Details | Ontario Health

Multiple Carboxylase Deficiency

Test Information

Title: Multiple Carboxylase Deficiency
Lab: Newborn Screening Ontario
Category: Metabolic
Test Name (CMS Title): Organic Acid Disorders
Gene/Platform/Region List: CA5A, HLCS, BTD
Test type
Samples Accepted: Blood, DNA, Dried Blood Spot (accepted ONLY for exceptional circumstances)
Indications: Diagnosis, Carrier Cascade Testing
Test Methodology: Sequencing
Disease/Condition: Carbonic Anhydrase Deficiency, Holocarboxylase Synthetase Deficiency, Biotinidase Deficiency

The information on this website is intended for informational purposes only and is not a substitute for medical advice. Always consult your health care provider if you have questions or concerns. The use of the information on this website does not create a physician-patient relationship between Ontario Health and you.
Ontario Health is committed to ensuring accessible services and communications to individuals with disabilities. To receive any information on this website in an alternate format, please contact Ontario Health’s Communications Department at: 1-877-280-8538,TTY 1-800-855-0511, or by email at info@ontariohealth.ca.