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Ildren March 2010 EXECUTIVE SUMMARY This White Paper provides a unique opportunity to reflect on how well one important segment of our public health system, newborn screening, functions within the current health care scheme, to identify gaps, and propose ways in which health reform might improve the quality and efficiency of public health programs overall for the benefit of the families that they serve. Nearly all of the 4 million infants born in the United States annually undergo newborn sc.
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17th FAQ
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The following are the common diseases detected in newborn screening using blood tests: Glucose-6 Phosphate Dehydrogenase Deficiency. Congenital Hypothyroidism. Congenital Adrenal Hyperplasia. Galactosemia. Phenylketonuria. Maple Syrup Urine Disease. Cystic Fibrosis. Biotinidase Deficiency.
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The newborn screenings your baby will most likely undergo include: A rating on the Apgar scale. ... A congenital heart disease screening. ... 21 or more types of blood screens. ... A hearing test. ... Blood test. ... Congenital heart disease screening. ... Newborn hearing screening.
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What are newborn screening tests? 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.
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Each year, millions of babies in the U.S. are routinely screened, using a few drops of blood from the newborn's heel, for certain genetic, endocrine, and metabolic disorders, and are also tested for hearing loss and critical congenital heart defects (CCHDs) prior to discharge from a hospital or birthing center. Newborn Screening Portal | CDC cdc.gov https://.cdc.gov › newbornscreening cdc.gov https://.cdc.gov › newbornscreening
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Screening for RUSP Conditions To date, a total of 37 conditions make up the RUSP, plus screening for hearing loss. Many states also screen for secondary conditions, which are other serious diseases detectable at birth via NBS.
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Metabolic disorders in newborn screening include: phenylketonuria (PKU) methylmalonic acidemia. maple syrup urine disease (MSUD) tyrosinemia. citrullinema. medium chain acyl CoA dehydrogenase (MCAD) deficiency. Newborn Screening Tests (for Parents) | Nemours KidsHealth kidshealth.org https://kidshealth.org › parents › newborn-screening-tests kidshealth.org https://kidshealth.org › parents › newborn-screening-tests
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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. Newborn Screening Tests | Children's Hospital of Philadelphia chop.edu https://.chop.edu › conditions-diseases › newborn-s... chop.edu https://.chop.edu › conditions-diseases › newborn-s...
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The RUSP is a guideline that helps states decide which conditions to include on their newborn screening panels. Each state makes its own decision about what their panels will include (or not include). Most states screen for most conditions on the RUSP. Recommended Uniform Screening Panel - Newborn Screening - HRSA hrsa.gov https://newbornscreening.hrsa.gov › recommended-unifo... hrsa.gov https://newbornscreening.hrsa.gov › recommended-unifo...
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Learn more -
Common neonatal syndromes
by MH Lipson · 2005 · Cited by 11 — This condition, a disorder of collagen metabolism...
Learn more -
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