NBS New Panel(CH, CAH, G6PD, Galactose)
- Thyroid Stimulating Hormone
- Total Galactose
- 17-alpha-hydroxyprogesterone
- Glucose-6-phosphate Dehydrogenase
The Newborn Screening (NBS) New Panel is an advanced screening test that detects a wide range of inherited metabolic, genetic, and endocrine disorders in newborns. The expanded panel screens for over 50 conditions, including PKU, hypothyroidism, cystic fibrosis, and sickle cell anemia.
All newborns are recommended to undergo this test between 24–72 hours after birth to ensure early detection of potentially life-threatening conditions.
A few drops of blood are collected from the newborn’s heel (heel-prick) and placed on a filter paper card. The sample is analyzed using tandem mass spectrometry (MS/MS) or other molecular techniques.
- Normal result: No abnormality detected.
- Abnormal result: Indicates the presence of a metabolic or genetic disorder, requiring further diagnostic testing.
Early detection allows for timely intervention, preventing severe complications, disability, or death.
Test code
7517
CPT and Loinc codes
Department
- Eia-neonatal
Turn around time
Next Day
Performing locations
1 labs across India
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.
Package price
₹1300
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₹1300