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DNA Labs India

GLDC Gene Glycine encephalopathy NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

GLDC Gene Glycine encephalopathy NGS Genetic Test

Also known as: Glycine Encephalopathy, Nonketotic Hyperglycinemia

GLDC Gene Glycine encephalopathy NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood, Extracted DNA, FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

Next-Generation Sequencing (NGS)All Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the GLDC Gene Glycine Encephalopathy NGS Genetic Test is to confirm the diagnosis of glycine encephalopathy by detecting mutations in the GLDC gene. This test helps in identifying carriers, guiding treatment decisions, and providing genetic counseling for affected families.

Test Code
5406
Price
₹20,000
Sample Type
Blood, Extracted DNA, FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Provide clinical history and undergo genetic counseling.

Step 2

Laboratory Analysis

Your sample is analyzed using Next-Generation Sequencing (NGS) 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 to 4 Weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor and provide medical history.
2
During the Test:Sample collection via blood draw or DNA extraction.
3
After the Test:Wait for results in 3-4 weeks. Genetic counseling for interpretation.

About This Test

Who Should Get This Test

The purpose of the GLDC Gene Glycine Encephalopathy NGS Genetic Test is to confirm the diagnosis of glycine encephalopathy by detecting mutations in the GLDC gene. This test helps in identifying carriers, guiding treatment decisions, and providing genetic counseling for affected families.

How to Prepare

  • Blood sample
  • Extracted DNA
  • FTA Card with one drop of blood

Doctor's Notes

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

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood, Extracted DNA, FTA Card

Understanding Your Results

Results indicate the presence or absence of mutations in the GLDC gene associated with glycine encephalopathy.
📊

Positive for pathogenic variants

Confirms diagnosis of glycine encephalopathy. Genetic counseling recommended.

📊

Negative

No mutations detected. Clinical correlation advised.

⚠️ When to Consult a Doctor:

If symptoms such as developmental delay, seizures, or muscle stiffness are present, or if there is a family history of glycine encephalopathy.

Risks & Considerations

  • Minor bruising at blood draw site
  • Psychological impact of results

Frequently Asked Questions

What is GLDC Gene Glycine Encephalopathy?
GLDC gene glycine encephalopathy is a rare genetic disorder caused by mutations in the GLDC gene, leading to glycine accumulation and nervous system issues.
What are the symptoms of glycine encephalopathy?
Symptoms include developmental delay, seizures, muscle stiffness, difficulty breathing, abnormal eye movements, low muscle tone, and feeding difficulties.
How is the test performed?
The test uses next-generation sequencing (NGS) to analyze DNA from blood or other samples for mutations in the GLDC gene.
What is the cost of the test?
The cost is INR 20,000, with free home sample collection available across India.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings in numerous cities.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What does a positive result mean?
A positive result confirms the presence of pathogenic GLDC gene mutations, indicating glycine encephalopathy. Genetic counseling is recommended.
Can this test be used for carrier screening?
Yes, it can identify carriers of GLDC gene mutations, aiding in family planning and genetic counseling.
Is genetic counseling included?
Yes, genetic counseling is part of the testing process to help interpret results and provide guidance.
What are the risks of the test?
Risks are minimal, such as minor bruising from blood draw, and potential psychological impact of results.
How accurate is the NGS test?
NGS is highly accurate for detecting genetic mutations, but accuracy depends on sample quality and laboratory standards.
What should I do if I have a family history of the disorder?
Consult a healthcare professional for genetic counseling and consider testing for early diagnosis and management.
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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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

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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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