Neonatal Karyotyping
Overview of Neonatal Karyotyping in Aluva
What is Neonatal Karyotyping?
This test analyzes the chromosomes of newborns to detect genetic abnormalities, such as Down syndrome or other chromosomal anomalies.
Why is the test performed?
It is used in neonates with congenital anomalies, developmental delays, or ambiguous genitalia for diagnostic and prognostic purposes.
What sample is needed, and how is it collected?
A blood sample from the newborn is cultured and analyzed under a microscope to assess chromosome number and structure.
How are the results interpreted?
Abnormal karyotypes suggest specific chromosomal syndromes. Findings can guide further genetic counseling and management.
Is any special preparation needed before the test?
No special preparation is needed. Timely collection and transport of the blood sample are essential.
Test included
- Specimen
- Indications
- Cells Counted & Analysed
- Cells Karyotyped
- Karyotype
Doctor information
Test code
5815
CPT and Loinc codes
Department
- Cytogenetics
Turn around time
10 Working Days
Test run frequency
Every Day TIME - 07:00
Performing locations
2 labs across India
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Heparin Whole Blood | Green Vacutainer | 2 ML |
Specimen stability information
Heparin Whole Blood
Collection instructions
Whole Blood-Heparin Specimen To Reach Us In 24 – 48 Hrs / Cord Blood- Heparin (If Baby Is Alive)+Clinical History In Specified Format
Test price
₹3500
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