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They may order genetic tests to find out if you have primary (inherited) or secondary trimethylaminuria

They may have additional recommendations to support any treatment that the person needs and can help them avoid possible reactions and interactions

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Product advantages Simple SUAC determination with upgrade set Screening for many metabolic disorders in a single run such as PKU (Phenylketonuria), MSUD (Maple Syrup Urine Disease) and tyrosinemia type I Each analyte safeguarded by its own internal standard Assay characteristics This Chromsystems assay allows the fast determination of amino acids and acylcarnitines from dried blood spot samples as part of the newborn screening for amino acid and fatty acid metabolic disorders using tandem mass spectrometry