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DNA Labs India

Neuronal Ceroid Lipofuscinosis Gene Panel Test

DNA Labs India | ISO 9001:2015 Certified

Neuronal Ceroid Lipofuscinosis Gene Panel Test

Short Name: NCL Gene Panel

Also known as: Batten Disease, NCL

Neuronal Ceroid Lipofuscinosis Gene Panel Test test available at DNA Labs India for ₹36,000. Uses Next-Generation Sequencing (NGS) on Amniotic fluid, Chorionic villi, Peripheral blood samples. Results in 4-6 weeks. Free home collection in 300+ cities across India.

Genetic Panel🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Neuronal Ceroid Lipofuscinosis Gene Panel is to identify pathogenic genetic mutations responsible for NCL, enabling definitive diagnosis, informing treatment strategies, facilitating genetic counseling for families, and supporting early intervention to manage symptoms and improve patient outcomes.

Test Code
3111
Price
₹36,000
Sample Type
Amniotic fluid, Chorionic villi, Peripheral blood
Result Time
4-6 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Neuronal Ceroid Lipofuscinosis Gene Panel can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Method: Varies by sample type: venipuncture for blood, amniocentesis for amniotic fluid, chorionic villus sampling for chorionic villi

Step 2

Laboratory Analysis

Standard sample collection procedures followed by healthcare professionals.

Step 3

Report Delivery

Sample is transported to the laboratory under appropriate conditions for genetic analysis.

Timeline: 4-6 weeks

Patient Instructions

1
Before the Test:Obtain a doctor's prescription, except for surgery, pregnancy, or travel abroad cases. No fasting required.
2
During the Test:Sample collection performed by trained personnel using sterile techniques.
3
After the Test:Sample sent to laboratory; results available in 4-6 weeks.

About This Test

Who Should Get This Test

The purpose of the Neuronal Ceroid Lipofuscinosis Gene Panel is to identify pathogenic genetic mutations responsible for NCL, enabling definitive diagnosis, informing treatment strategies, facilitating genetic counseling for families, and supporting early intervention to manage symptoms and improve patient outcomes.

How to Prepare

  • Use sterile containers as specified
  • Maintain cool pack for sample transport
  • Ensure proper labeling and documentation

Doctor's Notes

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

"Genetic testing is crucial for early diagnosis and management of Neuronal Ceroid Lipofuscinosis. Families with a history should consider genetic counseling for informed decision-making."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeAmniotic fluid, Chorionic villi, Peripheral blood
ContainerSterile container, Sterile Normal Saline Container, EDTA Vacutainer
Collection MethodVaries by sample type: venipuncture for blood, amniocentesis for amniotic fluid, chorionic villus sampling for chorionic villi

Sample Stability

Peripheral blood: stable for 48 hours at 2-8°C
Amniotic fluid and chorionic villi: follow laboratory-specific guidelines
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improper container or labeling

Understanding Your Results

Results from the Neuronal Ceroid Lipofuscinosis Gene Panel indicate the presence or absence of genetic mutations associated with NCL, guiding clinical diagnosis and management.
📊

Positive for pathogenic variant

Confirms genetic diagnosis of NCL; recommend genetic counseling and clinical management.

📊

Negative for pathogenic variants

No mutations detected in tested genes; clinical correlation and further testing may be needed.

📊

Variant of uncertain significance

Genetic variant identified but clinical significance unclear; recommend follow-up and family studies.

⚠️ When to Consult a Doctor:

Consult a doctor if symptoms of NCL such as vision loss, seizures, or developmental regression are present, or if there is a family history of the disorder.

Limitations

  • May not detect all genetic variants or novel mutations
  • Requires clinical correlation for diagnosis
  • Genetic counseling is essential for interpretation

Risks & Considerations

  • Minimal risk from sample collection (e.g., bruising for blood draw)
  • Genetic privacy and psychological impact of results

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Incorrect sample type

Compare With Similar Tests

TestNeuronal Ceroid Lipofuscinosis Gene PanelSingle Gene Test for NCLWhole Exome SequencingNeurological Genetic PanelEnzyme Assay for NCL
ComparisonNeuronal Ceroid Lipofuscinosis Gene Panel

Frequently Asked Questions

What is Neuronal Ceroid Lipofuscinosis (NCL)?
NCL, or Batten disease, is a rare genetic disorder affecting the nervous system, leading to progressive loss of vision, motor skills, and cognitive function.
What does the Neuronal Ceroid Lipofuscinosis Gene Panel test for?
This test identifies mutations in genes associated with the 13 types of NCL, aiding in diagnosis and genetic counseling.
What is the cost of the test in India?
The cost is INR 36000, and it is not covered by insurance. Home collection is available at no extra charge.
What samples are required for the test?
Samples can include peripheral blood, amniotic fluid, or chorionic villi, collected in sterile containers.
How long does it take to get results?
Results are typically available within 4-6 weeks after sample collection.
Is fasting required before the test?
No, fasting is not required for this genetic test.
Who should consider this test?
Individuals with symptoms of NCL, such as vision loss or seizures, or those with a family history of the disorder.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection across many cities in India.
What if the test results are positive?
A positive result confirms a genetic diagnosis of NCL; genetic counseling and clinical management are recommended.
Can this test be done during pregnancy?
Yes, it can be performed on amniotic fluid or chorionic villi samples, but a doctor's prescription is required.
What is the accuracy of the test?
The test uses Next-Generation Sequencing (NGS) for high accuracy, but genetic counseling is advised for interpretation.
How do I book the test?
You can book online through DNA Labs India's website or contact them via phone or WhatsApp for assistance.
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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For Hospitals & Clinics

Reference Laboratory Services

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.

LIMS Integration

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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