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DNA Labs India

William's Syndrome (FISH) Test

DNA Labs India | ISO 9001:2015 Certified

William's Syndrome (FISH) Test

William's Syndrome (FISH) Test test available at DNA Labs India for ₹5,250. Uses FISH on Peripheral blood/Amniotic fluid/Chorionic villi/Cord blood samples. Results in 3-4 days. Free home collection in 300+ cities across India.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the William's Syndrome FISH test is to detect the deletion of genetic material on chromosome 7, which is responsible for causing William's Syndrome. This test aids in confirming diagnosis, guiding management, and facilitating early intervention to address symptoms and improve patient outcomes.

Test Code
3234
Price
₹5,250
Sample Type
Peripheral blood/Amniotic fluid/Chorionic villi/Cord blood
Result Time
3-4 days
Fasting Required
No
Method
FISH
Step 1

Sample Collection

A doctor's prescription is required for the test. Prescription is not applicable for surgery, pregnancy cases, or people planning to travel abroad.

Step 2

Laboratory Analysis

Your sample is analyzed using FISH in our laboratory.

Step 3

Report Delivery

A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.

Timeline: 3-4 days

Patient Instructions

1
Before the Test:A doctor's prescription is required. Ensure sample is collected in appropriate containers and transported correctly.

About This Test

Who Should Get This Test

The purpose of the William's Syndrome FISH test is to detect the deletion of genetic material on chromosome 7, which is responsible for causing William's Syndrome. This test aids in confirming diagnosis, guiding management, and facilitating early intervention to address symptoms and improve patient outcomes.

How to Prepare

  • Use a sterile container, sterile normal saline container, or sodium heparin vacutainer (2ml)
  • Maintain sample at ambient or cool pack temperature during transport

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Early diagnosis through FISH testing is crucial for managing William's Syndrome and improving quality of life with timely interventions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypePeripheral blood/Amniotic fluid/Chorionic villi/Cord blood
ContainerSterile container/Sterile Normal Saline Container/Sodium heparin Vacutainer (2ml)

Understanding Your Results

Results from the FISH test indicate whether a deletion on chromosome 7 is present, which is diagnostic for William's Syndrome.
Positive result: Deletion detected on chromosome 7, consistent with William's Syndrome diagnosis
Negative result: No deletion detected, suggesting absence of William's Syndrome genetic cause
⚠️ When to Consult a Doctor:

Consult a doctor if your child exhibits symptoms such as distinctive facial features, developmental delays, heart problems, or intellectual disability, as early diagnosis and intervention can significantly improve outcomes.

Frequently Asked Questions

What is William's Syndrome?
William's Syndrome is a rare genetic disorder caused by a deletion of genetic material on chromosome 7, leading to physical and intellectual disabilities.
What causes William's Syndrome?
It is caused by a deletion of genetic material on chromosome 7, which affects multiple genes and leads to the characteristic features of the syndrome.
What are the common symptoms of William's Syndrome?
Symptoms include distinctive facial features, intellectual disability, developmental delays, short stature, heart problems, and anxiety or hyperactivity.
How is William's Syndrome diagnosed?
Diagnosis involves physical examination, genetic testing such as FISH to detect chromosome 7 deletion, and echocardiograms to assess heart issues.
What is the FISH test for William's Syndrome?
FISH (Fluorescence In Situ Hybridization) is a genetic test that detects the deletion on chromosome 7 responsible for William's Syndrome.
What is the cost of the FISH test at DNA Labs India?
The cost of the FISH test for William's Syndrome at DNA Labs India is INR 5250.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for online bookings across India.
How long does it take to get the results?
Reports are typically available within 3-4 days after sample collection.
What samples are required for the test?
Samples can include peripheral blood, amniotic fluid, chorionic villi, or cord blood, collected in sterile containers.
Is a doctor's prescription needed for the test?
Yes, a doctor's prescription is required, except for surgery, pregnancy cases, or people planning to travel abroad.
Can the test be done during pregnancy?
Yes, the test can be performed using amniotic fluid or chorionic villi samples during pregnancy, but a doctor's prescription is not applicable in such cases.
What are the treatment options for William's Syndrome?
Treatment focuses on managing symptoms through early intervention, therapies, and medical care for associated conditions like heart problems.
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 Data Privacy

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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