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The expanded newborn screening program increased the screening panel of disorders from six (6) to more than twenty-eight.
Newborn screening program in the Philippines currently includes screening of six disorders: Congenital Hypothyroidism (CH), Congenital Adrenal Hyperplasia (CAH), Phenylketonuria (PKU), Galactosemia (GAL), Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency and Maple Syrup Urine Disease (MSUD).
Soon after birth a few drops of blood are taken from your babys heel. These blood spots are used for newborn screening. This program is required by state law and screens all babies for rare but serious disorders to ensure early treatment.
Newborn screening tests may include: Phenylketonuria (PKU). PKU is an inherited disease in which the body cannot metabolize a protein called phenylalanine. Congenital hypothyroidism. Galactosemia. Sickle cell disease. Maple syrup urine disease. Homocystinuria. Biotinidase deficiency. Congenital adrenal hyperplasia.
Michigan law mandates NBS. Appendix 1 summarizes NBS legislation. If parents will not permit collection of the screen, it is suggested that the hospital request that parents sign a waiver stating that they were informed of the risk to their newborn if screening is declined and return the form to the NBS Program.
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The Michigan Newborn Screening Program tests for more than 50 medical conditions. The Michigan Department of Health and Human Services works with hospitals and midwives to make sure babies are screened and assure that children with a disorder receive proper treatment.
Please call 517-335-1400 to see if you qualify for a free screening.

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