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DNA Labs India

Chromosomes 18, X & Y Test

DNA Labs India | ISO 9001:2015 Certified

Chromosomes 18, X & Y Test

Also known as: FISH for Chromosomes 18, X, Y, Chromosome 18 and Sex Chromosome Analysis

Chromosomes 18, X & Y Test test available at DNA Labs India for ₹6,000. Uses FISH (Fluorescence In Situ Hybridization) on Amniotic fluid / Chorionic villi / Cord blood samples. Results in 3-4 days. Free home collection in 300+ cities across India.

Genetic TestingAll ages, including prenatal🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of Chromosomes 18, X & Y testing is to detect numerical abnormalities in chromosomes 18, X, and Y, which can cause genetic disorders. This aids in diagnosis, prognosis, and informed decision-making for patients and families.

Test Code
2967
Price
₹6,000
Sample Type
Amniotic fluid / Chorionic villi / Cord blood
Result Time
3-4 days
Fasting Required
No
Method
FISH (Fluorescence In Situ Hybridization)
Step 1

Sample Collection

A doctor's prescription is required for this test, except in cases of surgery, pregnancy, or travel abroad. No specific preparation is needed, but patients should inform their healthcare provider of any medications or conditions.

Method: As per sample type, typically invasive for prenatal samples

Step 2

Laboratory Analysis

Sample collection is performed by trained professionals. For amniotic fluid or chorionic villi, it is an invasive procedure done under ultrasound guidance.

Step 3

Report Delivery

After sample collection, apply pressure to the site if needed. Monitor for any signs of infection or discomfort and follow post-procedure instructions from the healthcare provider.

Timeline: 3-4 days

Patient Instructions

1
Before the Test:Obtain a doctor's prescription. Inform the healthcare provider of any medical history or current conditions.
2
During the Test:Sample collection is performed in a clinical setting. For invasive procedures, local anesthesia may be used.
3
After the Test:Rest and monitor for any side effects. Results will be available in 3-4 days.

About This Test

Who Should Get This Test

The purpose of Chromosomes 18, X & Y testing is to detect numerical abnormalities in chromosomes 18, X, and Y, which can cause genetic disorders. This aids in diagnosis, prognosis, and informed decision-making for patients and families.

How to Prepare

  • Ensure sterile collection conditions
  • Use appropriate containers as specified
  • Label samples correctly with patient details
  • Transport samples at ambient or cool temperature as indicated

Doctor's Notes

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

"This test is essential for early detection of chromosomal abnormalities, aiding in timely intervention and management for conditions like Trisomy 18 and sex chromosome disorders."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeAmniotic fluid / Chorionic villi / Cord blood
ContainerSterile container / Sterile Normal Saline Container / Sodium heparin Vacutainer (2ml)
Collection MethodAs per sample type, typically invasive for prenatal samples

Sample Stability

Amniotic fluid: Stable for 24-48 hours at room temperature
Chorionic villi: Stable for 24 hours at 4°C
Cord blood: Stable for 48 hours at room temperature
Sample Rejection Criteria:
  • Contaminated samples
  • Insufficient sample volume
  • Improper labeling or container

Understanding Your Results

Results from Chromosomes 18, X & Y testing indicate the presence or absence of chromosomal abnormalities. Abnormal results may suggest genetic disorders, requiring further evaluation and genetic counseling.
📊

Normal

No abnormalities detected in chromosomes 18, X, and Y. Further testing may not be needed unless symptoms persist.

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Abnormal - Trisomy 18

Three copies of chromosome 18 detected, indicating Edwards syndrome. Associated with severe developmental issues and often poor prognosis.

📊

Abnormal - Sex Chromosome Aneuploidy

Variations in X or Y chromosomes, such as XXX, XXY, or XYY, which may lead to conditions like Turner or Klinefelter syndrome with variable symptoms.

⚠️ When to Consult a Doctor:

Consult a doctor if test results are abnormal, if symptoms like developmental delays or recurrent infections persist, or for genetic counseling and management options.

Limitations

  • FISH may not detect all chromosomal abnormalities, such as subtle structural changes
  • Limited to specific chromosomes (18, X, Y); comprehensive karyotyping may be needed for full analysis

Risks & Considerations

  • For invasive samples: Risk of infection, miscarriage (for amniocentesis), or discomfort
  • Minimal risks for non-invasive samples like cord blood

Interfering Factors

  • Sample contamination
  • Poor sample quality
  • Technical errors in FISH procedure

Frequently Asked Questions

What is Chromosomes 18, X & Y testing?
It is a genetic test using FISH to detect abnormalities in chromosomes 18, X, and Y, helping diagnose conditions like Trisomy 18 and sex chromosome disorders.
Why is this test recommended?
It is recommended for individuals with symptoms such as developmental delays, intellectual disability, or abnormal facial features, or for prenatal screening.
How is the test performed?
The test involves collecting samples like amniotic fluid, chorionic villi, or cord blood, which are analyzed using FISH technology in a laboratory.
What is the cost of the test?
The test costs INR 6000 at DNA Labs India, with free home sample collection available.
Is fasting required before the test?
No, fasting is not required for this test.
How long does it take to get results?
Results are typically available within 3-4 days after sample collection.
What do abnormal results mean?
Abnormal results indicate chromosomal abnormalities, which may be associated with genetic disorders. Consult a doctor for interpretation and next steps.
Are there any risks associated with the test?
For invasive samples, there are minor risks like infection or discomfort. Discuss with your healthcare provider.
Can this test be done during pregnancy?
Yes, it can be performed prenatally using amniotic fluid or chorionic villi samples, but requires a doctor's prescription.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings across many cities in India.
What should I do if I have symptoms of a chromosomal disorder?
Consult a healthcare provider who may recommend this test or other evaluations based on your symptoms.
How accurate is the FISH method for this test?
FISH is a highly accurate method for detecting numerical abnormalities in specific chromosomes, but it may not detect all types of genetic changes.
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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Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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