CP 520-LS (CH )
Test Name
CP 520-LS (CH )
Lab Visit
Test Code
NBS012
Test Components/ Genes/ Parameters
CH
Sample Report
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Test Information
TAT DETAILS
48 Hrs
PRE-TEST INSTRUCTIONS
NA
CLINICAL UTILITY
To detect metabolic disorders or inborn errors of metabolism
To identify early signs of congenital hypothyroidism (CH)
To evaluate treatment effectiveness
To screen newborns for potential health conditions
SPECIMEN STABILITY
NA
METHODOLOGY
TRFA
STORAGE TEMPERATURE
NA
SPECIMEN TYPE
DBS/Filter Paper- 4 Spots
Frequently Asked Questions
To detect metabolic disorders or inborn errors of metabolism
meaures the level of CH in your newborn’s Blood
test is recommended for all newborns between the ages of 48 hours and 5 days
the baby has a family history of metabolic disorders or inborn errors of metabolism,
the baby shows symptoms such as poor feeding, lethargy, vomiting, or seizures, or
the mother has had metabolic disorders or if there were complications during pregnancy.
If any of the analyte levels are significantly high or low, it may indicate a metabolic disorder or an inborn error of metabolism. Further confirmatory testing will be required, and the child may need treatment.