in order to detect diseases early and stop its progression and fix the problem so that when you grow up, the complications will be fixed and no more signs that will be seen in you.
Newborn Screening
This has nothing to do with Christianity as it is written. Please add more to the question.
If you can prove it you would need to sue the hospital.
newborn screening is done in babies to detect for any birth defects.. its better to take preventive measures than to regret later, because babies who have any birth defects and the babies who do not have look same at birth, it is only when the symptoms appears one can come to know about the disease but that sometimes may be too late for the treatment and that often leads to death of infants, which can be avoided if newborn screening is done at the time of birth.
A newborn screening test for cystic fibrosis typically detects the presence of elevated levels of immunoreactive trypsinogen (IRT) in the blood, which can indicate the condition. However, a newborn can only have cystic fibrosis if both parents are carriers of the defective CFTR gene. If only one parent is a carrier, the child will not inherit the disease, but may still be tested as a carrier. Therefore, a positive newborn screening result may indicate the need for further testing to confirm the diagnosis.
Comprehensive panel metabolic screening is done on newborn babies to test for genetic disorders from birth. The panel comprises of many rare metabolic disorders which individually might occure very rare but when seen collectively the occurrence increase many fold. There are more than 100 metabolic disorders which can be detected in a newborn urine sample.
Babies seem to do okay with newborn screenings. It is a tiny bit painful, but most babies do okay after the initial testing point is over, especially the heel pricks.
The author of Republic Act 9288, also known as the "Newborn Screening Act," is the Congress of the Philippines. The act was enacted on March 21, 2004, and aims to promote early detection and prevention of certain diseases in newborns through screening programs.
no :/
They will do more than one test to absolutly make sure, and you would get the treatment as soon as possible.
Your best bet to get an answer is to ask a nurse, doctor, or anyone else in the medical field. They would most likely know since they work with this subject. Newborn Genetic Screening is a very simple painless test for every newborn. All it requires are few drops of urine and the bay gets covered for over 100 metabolic disorders. This test is usually diagnostic and treatment can be instituted as soon as possible by the doctor. This test is fairly easy to interpret and test results are available to parents too. You may also order the test online as it is also offered Direct to Home to parents. In case the test comes out positive then the doctors come in to picture to start the treatment.
LCMS (actually) LCMS/MS goes the half way for newborn screening. Its then the GCMS which comes for rescue. It clarifies the results given by LCMS and says with accuracy whether it is a positive or a negative case, against what was indicated in the LCMS screening. GCMS is mostly based on urine sample while LCMS needs blood spots. Thats where GCMS already scores a big point above LCMS. Further, GCMS "confirms" a disorder, while LCMS stops at "maybe". GCMS tests for a massive range of disorders while LCMS is limited to a few class of disorders. GCMS is the future of screening, while LCMS is the present of screening.