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FISH - Amnio Three Probes: Trisomy 18 X & Y Test

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FISH - Amnio Three Probes: Trisomy 18 X & Y Test

Short Name: FISH Trisomy 18 XY Test

Also known as: FISH for Trisomy 18, FISH X & Y Probes Test

FISH - Amnio Three Probes: Trisomy 18 X & Y Test test available at DNA Labs India for ₹10,500. Uses FISH, Fluorescence In Situ Hybridization on Amniotic fluid samples. Results in Reports are ready within 4 days after sample collection.. Free home collection in 300+ cities across India.

Diagnostic TestFemaleAdult🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to provide rapid prenatal diagnosis for trisomy 18 and sex chromosome abnormalities, such as monosomy X, to guide clinical management and informed decision-making during pregnancy.

Test Code
569
Price
₹10,500
Sample Type
Amniotic fluid
Result Time
Reports are ready within 4 days after sample collection.
Fasting Required
No
Method
FISH, Fluorescence In Situ Hybridization
Step 1

Sample Collection

Patient must be after 15 weeks gestation. Duly filled Prenatal Genetic Testing Consent Form (Form 18) and Chromosome & FISH Analysis Requisition Form (Form 17) are mandatory. Discuss risks and benefits with the healthcare provider.

Method: Amniocentesis

Step 2

Laboratory Analysis

Amniocentesis is performed under ultrasound guidance. A thin needle is inserted through the abdomen to withdraw 10-20 mL of amniotic fluid. The procedure takes about 10-15 minutes.

Step 3

Report Delivery

Monitor for signs of infection, leakage, or contractions. Avoid strenuous activity for 24 hours. Report any symptoms like fever, severe pain, or fluid leakage to the doctor immediately.

Timeline: Reports are ready within 4 days after sample collection.

Patient Instructions

1
Before the Test:Consult with a gynecologist or genetic counselor. Ensure gestation is after 15 weeks. Complete required consent forms. Avoid blood-thinning medications if advised.
2
During the Test:Amniocentesis procedure; may feel slight discomfort or pressure. Follow healthcare provider's instructions.
3
After the Test:Rest for a day, monitor for symptoms. Results are typically available in 4 days.

About This Test

Who Should Get This Test

The purpose of this test is to provide rapid prenatal diagnosis for trisomy 18 and sex chromosome abnormalities, such as monosomy X, to guide clinical management and informed decision-making during pregnancy.

How to Prepare

  • Sample must be taken after 15 weeks gestation
  • Collect 10 mL (7 mL min.) of amniotic fluid in a sterile screw capped container
  • Ship at 18-22°C; do not freeze
  • Complete mandatory forms: Prenatal Genetic Testing Consent Form (Form 18) and Chromosome & FISH Analysis Requisition Form (Form 17)

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"This FISH test provides rapid and accurate prenatal diagnosis for trisomy 18 and sex chromosome issues, aiding in early decision-making for high-risk pregnancies."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeAmniotic fluid
Sample Volume10 mL (7 mL min.)
ContainerSterile screw capped container
Collection MethodAmniocentesis

Sample Stability

Room Temperature
Refrigerator
Frozen
Sample Rejection Criteria:
  • Sample frozen
  • Inadequate volume
  • Non-sterile container
  • Missing consent or requisition forms
  • Sample collected before 15 weeks gestation

Understanding Your Results

Results indicate the presence or absence of trisomy 18 and abnormalities in X and Y chromosomes. Positive results require confirmation with full karyotyping and genetic counseling.
📊

Normal: Two copies of chromosome 18, normal sex chromosomes

No aneuploidy detected for targeted chromosomes

📊

Trisomy 18 Detected

Three copies of chromosome 18; consistent with Edwards syndrome

📊

Sex Chromosome Abnormality Detected

Abnormalities such as monosomy X (Turner syndrome) or extra X/Y chromosomes

📊

Inconclusive

Insufficient cells or technical issues; repeat testing may be needed

⚠️ When to Consult a Doctor:

Consult a doctor if results are abnormal, if you experience complications after amniocentesis, or for genetic counseling to understand implications and options.

Limitations

  • Only detects targeted abnormalities (trisomy 18 and sex chromosomes)
  • Not a substitute for full chromosome karyotype analysis
  • May not detect mosaicism or structural abnormalities
  • Requires invasive procedure with associated risks

Risks & Considerations

  • Risk of miscarriage (approximately 0.1-0.3%)
  • Infection at puncture site
  • Leakage of amniotic fluid
  • Mild cramping or spotting
  • Needle injury to fetus (rare)

Interfering Factors

  • Contaminated or inadequate sample
  • Improper sample storage (e.g., frozen)
  • Maternal cell contamination
  • Low fetal cell count

Compare With Similar Tests

TestFISH - Amnio Three Probes: Trisomy 18 X & Y TestChorionic Villus Sampling (CVS)Non-Invasive Prenatal Testing (NIPT)Amniocentesis KaryotypeFISH for Other Chromosomes
ComparisonFISH - Amnio Three Probes: Trisomy 18 X & Y Test

Frequently Asked Questions

What is the FISH - Amnio Three Probes: Trisomy 18 X & Y Test?
It is a prenatal diagnostic test using FISH technology to detect trisomy 18 and abnormalities in X and Y chromosomes from amniotic fluid.
When is this test recommended?
It is recommended for pregnant women over 35, with abnormal ultrasound findings, family history of chromosomal disorders, or positive screening tests.
How is the sample collected?
Sample is collected via amniocentesis after 15 weeks gestation, where amniotic fluid is withdrawn under ultrasound guidance.
What is the cost of the test?
The test costs INR 10500, which includes home collection in many cities across India.
How long does it take to get results?
Results are typically available within 4 days after sample collection.
Are there any risks associated with the test?
Yes, amniocentesis carries a small risk of miscarriage, infection, or fluid leakage, but these are rare.
Is home sample collection available?
Yes, free home sample collection is available for online bookings in numerous cities across India.
What does a positive result mean?
A positive result indicates detection of trisomy 18 or sex chromosome abnormalities, requiring confirmation and genetic counseling.
Can this test detect all chromosomal issues?
No, it only targets trisomy 18 and X/Y chromosomes; full karyotyping is needed for comprehensive analysis.
Do I need to fast before the test?
No, fasting is not required for this test.
What documents are required for the test?
Duly filled Prenatal Genetic Testing Consent Form (Form 18) and Chromosome & FISH Analysis Requisition Form (Form 17) are mandatory.
Is the test covered by insurance?
Coverage depends on your insurance policy; check with your provider for details.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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