NBS Lite - 7P
The NBS LITE-7P test is a screening panel for seven common neonatal disorders, including CAH, G6PD deficiency, cystic fibrosis, and PKU. Early detection helps prevent severe health issues in newborns.
NBS Lite - 7P Package in Mangaluru Overview
About NBS Screening Panel test?
The NBS LITE - 7P is a newborn screening panel that tests for seven key metabolic and hormonal markers. It includes important parameters such as 17-Hydroxyprogesterone (17OH), Biotinidase (BIOT), Glucose-6-Phosphate Dehydrogenase (G6PD), Immunoreactive Trypsinogen (IRT), Phenylalanine (PHYL), Galactose (GALAC), and Thyroid Stimulating Hormone (TSH). This test identifies common congenital conditions early, including hormone imbalances, enzyme deficiencies, and metabolic disorders, which, if detected promptly, can be effectively managed to prevent serious health issues. Typically performed using a small blood sample, it is a vital tool for newborn health assessment.
Why consider NBS Screening Panel test?
This test is important for early detection of several common metabolic and hormonal disorders in newborns that can lead to serious health problems if left untreated. Identifying conditions like hormone imbalances, enzyme deficiencies, or metabolic issues early allows for timely medical intervention, which can prevent developmental delays and other complications.
Who should get NBS Screening Panel test done?
- Newborns, as part of routine screening to detect metabolic and hormonal disorders early
- Babies with a family history of metabolic, hormonal, or enzyme-related conditions
- Infants showing symptoms like poor feeding, jaundice, or developmental delays
More Information about NBS Screening Panel test
Early identification through this test supports prompt treatment plans that can improve growth and development outcomes. It is designed to be cost-effective and efficient, making it accessible for widespread newborn screening programs.
Other Names :- Newborn Screening Lite Panel (7 Parameters), 7-Parameter Newborn Health Panel
No special preparations needed
- Immunoreactive Trypsinogen (irt)
- Thyroid Stimulating Hormone
- Total Galactose
- 17-alpha-hydroxyprogesterone
- Phenylalanine
- Biotinidase Deficiency
- Glucose-6-phosphate Dehydrogenase
Test code
7708
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Blood Spot | NeoNatal Cards | 1 |
Specimen stability information
Blood Spot
Collection instructions
Complete CLINICAL HISTORY form including birth date & birth time.(Dried Blood spot should be ideally collected within 2nd and 5th day of life after birth).Avoid touching and smearing of the blood spots.The dried blood specimen should be transported or mailed to the laboratory as soon as they are dry (Minimum of 3 Hrs.) and no later than 24 hrs after collection.
Specimen rejection criteria
Test run frequency
'
Turn around time
Next Day
Performing locations
Department
- Eia-neonatal
CPT and Loinc codes
Package price
₹2600
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₹2600