Several: Phenylketonuria (PKU), congenital hypothyroidism, galactosemia, congenital adrenal hyperplasia, glucose-6-phosphate dehydrogenase deficiency, maple syrup urine disease, medium chain acyl-CoA dehydrogenase deficiency, homocystinuria, glutaric academia type I, isovaleric acidemia and methylmalonic academia. These 11 congenital metabolic disorders are included in the newborn screening program.
Answered 9/28/2016
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