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SECTION 1. Short Title. - This Act shall be known as the "Newborn Screening Act of 2004."
What is newborn screening? Newborn screening (NBS) is a simple procedure to find out if your baby has a congenital metabolic disorder that may lead to mental retardation and even death if left untreated.
SEC. 2. Declaration of Policy. - It is the policy of the State to protect and promote the right to health of the people, including the rights of children to survival and full and healthy development as normal individuals.
SEC. 12. Establishment and Accreditation of Newborn Screening Centers. The DOH shall ensure that Newborn Screening Centers are strategically located in order to be accessible to the relevant public. Newborn screening is available in participating health institutions (hospitals, lyingins, Rural Health Units and Health Centers).
SEC. 13. Establishment of a Newborn Screening Reference Center. - The NIH shall establish a Newborn Screening Reference Center SEC. 14. Quality Assurance. - The NIH Newborn Screening Reference Center shall be responsible for drafting and ensuring good laboratory practice standards for newborn screening centers SEC. 15. Database. - All Newborn Screening Centers shall coordinate with the NIH Newborn Screening Reference Center for consolidation of patient databases
What should be done when a baby is tested a positive NBS result? Babies with positive results should be referred at once to the nearest hospital or specialist for confirmatory testing and further management. Should there be no specialist in the area, the NBS secretariat office will assist its attending physician.
CH (Congenital Hypothyroidism)
Lack of thyroid hormone Baby may suffer from growth and mental retardation.
An endocrine disorder that causes severe salt loss, dehydration and abnormally high levels of male sex hormones in both boys and girls. If not detected and treated early, babies with CAH may die within 7-14 days.
GAL (Galactosemia)
A condition in which babies are unable to process galactose, Accumulation of excessive galactose in the body can cause problems including liver damage, brain damage and cataracts.
PKU (Phenylketonuria)
Rare condition in which the baby cannot properly use phenylalanine. Excessive accumulation of phenylalanine in the blood causes brain damage.
G6PD Deficiency
The body lacks the enzyme G6PD (Glucose-6Phosphate Dehydrogenase). Babies with this deficiency may have hemolytic anemia resulting from exposure to oxidative substances found in drugs, food and chemicals.
Thank you
References:
Pink brochure. Newborn Screening Reference Center - National Institutes of Health, University of the Philippines Manila. (e-mail: nbsadmin@gmail.com) Jomento C. 2010. Maple Syrup Urine Disease Kit Evaluation. Newborn Screening (Official Publication of the Newborn Screening Reference Center NIH-UP Manila). 14(1):8. 2009 Statistics on National Coverage and Performance and Incidence Rates of NBS Genetic Disorders. Newborn Screening (Official Publication of the Newborn Screening Reference Center NIH-UP Manila). 14(1):3. http://www.pia.gov.ph/news/index.php?article=1951373982998
Religious Traditions and Prenatal Genetic Counseling Rebecca Rae Anderson College of Public Health, University of Nebraska Medical CenterAm J Med Genet C Semin Med Genet. 2009 February 15; 151C(1): 5261. doi:10.1002/ajmg.c.30203.