| newborn screening |
Newborn screening is the process of testing newborn babies for treatable genetic, endocrinologic, metabolic and hematologic diseases. Robert Guthrie is given much of the credit for pioneering the earliest screening for phenylketonuria in the late 1960s using blood samples on filter paper obtained by pricking a newborn baby's heel on the second day of life to get a few drops of blood. ...
출처: en.wikipedia.org/wiki/Newborn_screening
|
|---|---|
| newborn screening |
a test done on every baby born in the United States within the first few days of life, to look for inherited, treatable, metabolic disorders.
출처: www.uchicagokidshospital.org/online-library/conten...
|
| newborn screening |
testing tissue samples from newborns to detect abnormalities which may be associated with disease.
출처: www.cs.uu.nl/people/ronnie/local/genome/n.html
|
| newborn screening |
The examination of blood samples from a newborn infant to detect disease-related abnormalities or deficiencies in gene products.
출처: www.knowledgene.com/public/glossary_content.php3
|
| newborn screening |
A public health screening program to screen newborns for the presence of certain metabolic or genetic conditions. Screening is done within days of birth to identify infants at increased risk for a specific genetic or endocrine disorder so that treatment can begin as soon as possible: when a newborn screening result is "out-of-the-expected range", further diagnostic testing is usually required to confirm or specify the results.
출처: www.health.state.mo.us/NewbornScreening/Glossary.h...
|