Examples of 'newborn screening' in a sentence
Meaning of "newborn screening"
Newborn screening is a medical process that involves testing infants shortly after birth to detect certain genetic, metabolic, or developmental disorders. These tests are usually performed using blood samples or other samples obtained from the newborn, and they aim to identify any potential health issues early on to enable timely intervention or treatment
How to use "newborn screening" in a sentence
Basic
Advanced
newborn screening
A newborn screening sample can still be taken.
Quality assurance program for newborn screening.
This is where newborn screening becomes problematic.
Four rare diseases added to newborn screening.
Newborn screening projects have been initiated.
The case for universal newborn screening.
Newborn screening is more than just a laboratory test.
She was diagnosed at birth through newborn screening.
Antenatal and newborn screening programmes.
Newborn screening is not the same as diagnostic testing.
Surveying parents about newborn screening educational materials.
A newborn screening test may find a heart defect.
They are also active in newborn screening.
Newborn screening programs.
Challenges for worldwide harmonization of newborn screening programs.
See also
About newborn screening.
Treatment after confirmation of abnormal newborn screening results.
Through newborn screening.
It is diagnosed in infancy through newborn screening.
Many countries have newborn screening programs for the disease.
It also provides resources on newborn screening.
We have newborn screening.
Cystic fibrosis can be diagnosed at birth through newborn screening.
Each condition found on the newborn screening panel is different.
Newborn screening is so important.
It also comprises the diseases on newborn screening tests.
Newborn screening tests detect most babies with galactosemia soon after birth.
Seven things parents want to know about newborn screening.
Concept of newborn screening.
Many of these disorders are now detected through routine newborn screening.
All information relating to the newborn screening program is considered confidential.
A reliable detection of these two forms of thalassemia is not feasible through newborn screening.
Most of the conditions identified through newborn screening are autosomal recessive genetic conditions.
Parents whose child has been diagnosed with a genetic disease on a newborn screening test.
A newborn screening test is available for the most common form of congenital adrenal hyperplasia.
All babies get this test as part of newborn screening.
A positive newborn screening result does not mean that your baby has congenital hypothyroidism.
Site offers education material and information on newborn screening disorders.
The newborn screening programs differ by country in number and nature of the screened syndromes.
Most states test newborn babies as part of their newborn screening programs.
The newborn screening test with mass spectrometry and research of urinary organic acids were normal.
Young children who have not gone through the newborn screening test.
Newborn screening screens infants a few days after birth to evaluate for evidence of treatable diseases.
Provides information and resources in the area of newborn screening and genetics.
Newborn screening programs have also expanded the information base available about some rare conditions.
The following videos were created to discuss newborn screening issues with patients.
Newborn screening programs in Brazil are also inadequate.
It is most often found at birth during routine newborn screening tests at the hospital.
This is why newborn screening for CPS is so important.
Links to websites of groups that study and provide information about newborn screening.
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Examples of using Newborn
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All newborn babies look like that
Safe motherhood and newborn health continued
Newborn infants with low birth weight
Examples of using Screening
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Instituting routine screening during prenatal consultation
Screening for cancer has taken place
The result of a screening decision can be that
