Neonatal FISH 13 & 21 (2 Probe)
Overview of Neonatal FISH 13 & 21 (2 Probe) in Alappuzha
What is the Neonatal FISH 13, 21, 2 Probe Test?
This test uses Fluorescence In Situ Hybridization (FISH) to detect chromosomal abnormalities associated with trisomies 13, 21, and 2, which are linked to genetic disorders such as Down syndrome.
Who should get this test?
This test is recommended for:
Newborns suspected of having chromosomal abnormalities.
Infants with congenital anomalies or developmental delays.
How is the test performed?
A blood sample or amniotic fluid is analyzed using fluorescent probes to identify chromosomal anomalies.
What do the results indicate?
Normal result: No chromosomal abnormalities detected.
Abnormal result: Suggests trisomy 13, 21, or 2, requiring further genetic counseling.
Why is this test significant?
Early diagnosis helps manage and provide specialized care for affected infants.
Test included
- Specimen
- Clinical Indications
- 1st Hybridization (green Chr 13)
- Total Number Of Cells Analyzed
- Interpretation
- 2nd Hybridization (orange Chr 21)
- Total Number Of Cells Analysed
- Interpretation
Doctor information
Test code
5815F
CPT and Loinc codes
Department
- Cytogenetics
Turn around time
5 Working Days
Test run frequency
Every Day TIME - 10:00
Performing locations
3 labs across India
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Blood Spot | NeoNatal Cards | 2 |
| Heparin Whole Blood | Green Vacutainer | |
| Tissue | Others | 1 NOS |
Specimen stability information
Blood Spot, Heparin Whole Blood, Tissue
Collection instructions
Specimen To Reach Us In 24 – 48 Hrs / Cord Blood- Heparin (If Baby Is Alive)+Clinical History In Specified Format
Test price
₹4000
Need Help?
Talk to our health experts for guidance on tests, reports, or bookings.
WhatsApp to Book TestNeonatal FISH 13 & 21 (2 Probe)
₹4000