Skip to main content
DNA Labs India

CLN8 Gene Ceroid lipofuscinosis neuronal type 8 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

CLN8 Gene Ceroid lipofuscinosis neuronal type 8 NGS Genetic Test

Short Name: CLN8 Gene Test

Also known as: CLN8 Disease, Neuronal Ceroid Lipofuscinosis Type 8

CLN8 Gene Ceroid lipofuscinosis neuronal type 8 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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.

Metabolic Disorders🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify mutations in the CLN8 gene for early diagnosis of Ceroid Lipofuscinosis Neuronal Type 8, facilitating timely treatment and management.

Test Code
1908
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
NGS Technology
Step 1

Sample Collection

No specific preparation required; provide clinical history and undergo genetic counseling if applicable.

Method: Blood sample or FTA Card collection

Step 2

Laboratory Analysis

Blood draw or application of one drop on FTA card, performed by a trained professional.

Step 3

Report Delivery

Apply pressure to the puncture site; store sample as instructed for stability.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Complete pre-test information, provide clinical history, and attend genetic counseling session.
2
During the Test:Sample collection via blood draw or FTA card; analysis using NGS technology.
3
After the Test:Wait for report delivery in 3-4 weeks; consult a healthcare provider for result interpretation.

About This Test

Who Should Get This Test

To identify mutations in the CLN8 gene for early diagnosis of Ceroid Lipofuscinosis Neuronal Type 8, facilitating timely treatment and management.

How to Prepare

  • Use sterile equipment for blood collection
  • Label samples accurately with patient details

Doctor's Notes

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

"Early genetic testing for CLN8 is crucial for timely intervention, family planning, and management of neuronal ceroid lipofuscinosis symptoms."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodBlood sample or FTA Card collection

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the CLN8 gene, aiding in diagnosis.
Positive result: Pathogenic variant detected, confirming CLN8 disorder
Negative result: No variants detected, but clinical correlation needed
Uncertain variant: Further testing or family studies recommended
⚠️ When to Consult a Doctor:

If symptoms like developmental delays, seizures, or vision loss occur, or if genetic testing results are positive.

Limitations

  • May not detect all possible genetic variants
  • Results require correlation with clinical findings

Risks & Considerations

  • Minor bruising or discomfort at blood draw site
  • Rare infection risk

Interfering Factors

  • Contaminated DNA samples
  • Improper sample collection or storage

Frequently Asked Questions

What is the CLN8 Gene NGS Genetic Test?
It is a next-generation sequencing test to detect mutations in the CLN8 gene, associated with neuronal ceroid lipofuscinosis type 8.
Who should consider this test?
Individuals with symptoms like developmental delays, seizures, or vision loss, or those with a family history of the disorder.
How is the test performed?
Through blood sample or FTA card collection, analyzed using NGS technology for accurate mutation detection.
What is the cost of the test?
The test costs INR 20,000, with home collection available across India.
How long does it take to get results?
Reports are delivered within 3 to 4 weeks via online portal, email, or WhatsApp.
Is fasting required before the test?
No, fasting is not required for this genetic test.
What are the symptoms of CLN8 disease?
Early symptoms include developmental delays, seizures, and visual impairment, progressing to severe neurological decline.
How is the disease diagnosed?
Through clinical evaluation, genetic testing like this NGS test, and imaging studies such as MRI.
Is home sample collection available?
Yes, free home collection is offered for online bookings in cities across India.
What if the test result is positive?
A positive result confirms CLN8 disorder; consult a healthcare provider for management and genetic counseling.
Are there any risks associated with the test?
Minimal risks, such as minor bruising from blood draw; overall safe and non-invasive.
How accurate is the NGS test?
NGS provides high accuracy for detecting CLN8 gene mutations, but results should be correlated with clinical findings.
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.

Related Tests

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.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.