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Acetaldehyde is then oxidized by acetaldehyde dehydrogenases (ALDH2, ALDH1B1 and ALDH1A1) to acetate

Assessment of the presenting signs and symptoms is important Blood and urine tests, as necessary Radiological imaging studies of the affected parts of the body Prenatal imaging studies If carnitine levels in blood are extremely low after molecular genetic testing is performed, a healthcare provider may suspect Carnitine Deficiency Syndrome

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Approach with accurate expectations: this is a dietary supplement that may offer some support through botanical ingredients