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ST3GAL3 Gene Early infantile epileptic encephalopathy type 15 NGS Genetic Test

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ST3GAL3 Gene Early infantile epileptic encephalopathy type 15 NGS Genetic Test

Short Name: ST3GAL3 EIEE Type 15 NGS Test

ST3GAL3 Gene Early infantile epileptic encephalopathy type 15 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

Genetic TestPediatric🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to identify pathogenic mutations in the ST3GAL3 gene associated with EIEE Type 15. Confirming the genetic cause aids in accurate diagnosis, prognosis assessment, and informed treatment planning. It also facilitates genetic counseling for family members regarding inheritance risks.

Test Code
1592
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
Next Generation Sequencing (NGS)
Step 1

Sample Collection

Clinical history of the patient and a genetic counseling session to draw a pedigree chart are required before sample collection.

Method: Venipuncture or FTA Card

Step 2

Laboratory Analysis

Sample collection via venipuncture or using an FTA card with one drop of blood. Home collection is available.

Step 3

Report Delivery

The sample is processed and analyzed using NGS technology. Results are reviewed and reported by qualified geneticists.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Undergo genetic counseling and provide clinical history. No fasting is required.
2
During the Test:Sample collection through blood draw or FTA card. Home collection service is available.
3
After the Test:Sample is sent for NGS analysis. Results are delivered in 3 to 4 weeks via online portal, email, or WhatsApp.

About This Test

Who Should Get This Test

The purpose of this test is to identify pathogenic mutations in the ST3GAL3 gene associated with EIEE Type 15. Confirming the genetic cause aids in accurate diagnosis, prognosis assessment, and informed treatment planning. It also facilitates genetic counseling for family members regarding inheritance risks.

How to Prepare

  • Provide clinical history and undergo genetic counseling
  • Sample type: Blood, extracted DNA, or one drop blood on FTA card
  • Ensure proper labeling and handling of the sample

Doctor's Notes

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

"Genetic testing for ST3GAL3 mutations can confirm diagnosis of EIEE Type 15, which is crucial for early intervention and family counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or FTA Card

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the ST3GAL3 gene. A positive result confirms EIEE Type 15, while a negative result may require further testing or clinical correlation.
Positive: Pathogenic variant detected – confirms diagnosis of EIEE Type 15.
Negative: No pathogenic variants – clinical correlation recommended; consider other genetic or non-genetic causes.
Variant of uncertain significance (VUS) – further evaluation and family studies may be needed.
⚠️ When to Consult a Doctor:

Consult a geneticist or neurologist if seizures, developmental delays, or other symptoms are observed in infants, or for genetic counseling after test results to understand inheritance and management.

Risks & Considerations

  • Minor bruising or soreness at the blood draw site
  • Very rare risk of infection

Frequently Asked Questions

What is ST3GAL3 Gene EIEE Type 15?
EIEE Type 15 is a rare genetic disorder caused by mutations in the ST3GAL3 gene, leading to early-onset seizures and neurological issues.
What are the symptoms of EIEE Type 15?
Common symptoms include seizures in infancy, developmental delay, intellectual disability, hypotonia, and vision problems.
How is the ST3GAL3 Gene NGS test performed?
The test uses Next Generation Sequencing to analyze the ST3GAL3 gene from a blood sample or extracted DNA.
What is the cost of the test?
The test costs INR 20000 at DNA Labs India, with free home sample collection available.
Is home sample collection available?
Yes, free home collection is offered across India for this test.
How long does it take to get results?
Results are typically available in 3 to 4 weeks after sample collection.
What do the results mean?
A positive result confirms EIEE Type 15, a negative result may indicate no pathogenic variants, and a VUS requires further evaluation.
Is genetic counseling required?
Yes, genetic counseling is recommended before testing to draw a pedigree chart and understand implications.
Can this test be done for adults?
The test is primarily for infants with symptoms, but it can be performed at any age if indicated by a specialist.
What are the risks of the test?
Risks are minimal, such as minor bruising at the blood draw site.
How accurate is the test?
NGS technology provides high accuracy for detecting mutations in the ST3GAL3 gene, but clinical correlation is essential.
What should I do after getting the results?
Consult your geneticist or neurologist to discuss results, management options, and family planning.
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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