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How is MCAD Diagnosed?
MCAD deficiency is usually diagnosed through newborn screening, which involves a blood test to check for elevated levels of certain fatty acids. Additional tests, such as urine organic acid analysis and genetic testing, can confirm the diagnosis.
Frequently asked queries:
What is MCAD?
How is MCAD Deficiency Inherited?
How is MCAD Diagnosed?
How Can Parents Manage MCAD?
Can MCAD Deficiency Be Prevented?
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Is Donor Milk a Viable Option?
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