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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.