To assist in diagnosing congenital metabolic disorders in infants, typically homocystinuria, maple syrup urine disease, phenylketonuria (PKU), tyrosinuria, and unexplained mental retardation.
Urine (10 mL) from a random or timed specimen collected in a clean plastic collection container with hydrochloric acid as a preservative.
(Method: Chromatography) There are numerous amino acids. Values vary, and the testing laboratory should be consulted for corresponding ranges.
Amino Acid Screen, Urine has been found in Davis's Lab & Diagnostic Tests
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