FISH FOR ANEUPLOIDY IN POC CHROMOSOMES 13,18,21,X,Y

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NABL Cap Accredited     
FISH for Aneuploidy in Products of Conception (POC) is a genetic test used to detect numerical chromosomal abnormalities. At Metropolis Healthcare, this test targets chromosomes 13, 18, 21, X, and Y using fluorescence in situ hybridization. It helps identify common aneuploidies associated with pregnancy loss. The results support clinicians in understanding genetic causes of miscarriage and guiding future pregnancy planning 

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Price: Rs. 8,480.00

Sample Type: Products of Conception

Fasting Not Required


Booking Procedure:
  1. Technician from Metropolis will be assigned for a home sample collection after booking confirmation.
  2. Sample will be collected by our technician at your address at given slot.
  3. You can make the payment to the technician at the time of collection
  4. Your sample will then be transported to the nearest collection center and will be centrifuged before sending to the lab for processing.
  5. Soft copy reports will be sent to your email address within 24 to 48 hours or as per defined TAT for Tests.

Frequently Asked Questions (FAQ's):

What does the FISH for aneuploidy in POC test include at Metropolis Healthcare?
It includes targeted FISH analysis for chromosomes 13, 18, 21, X, and Y in POC samples.

Why is this test recommended by Metropolis Healthcare?
It helps determine whether chromosomal aneuploidy was a cause of pregnancy loss.

Who should consider this test at Metropolis Healthcare?
It is recommended after recurrent or unexplained miscarriages.

What sample is required for this test at Metropolis Healthcare?
A Products of Conception (POC) tissue sample is required.

How does Metropolis Healthcare perform this FISH test?
Metropolis Healthcare uses validated FISH probes and standardized laboratory protocols.

How quickly are results available from Metropolis Healthcare?
FISH testing provides faster results compared to full karyotyping.

How should results from Metropolis Healthcare be used clinically?
Results should be interpreted by clinicians or genetic counselors to guide further evaluation

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