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Common Neurological/Neuromuscular Diseases Gene Panel Test

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Common Neurological/Neuromuscular Diseases Gene Panel Test

Common Neurological/Neuromuscular Diseases 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.

Gene Panel🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr Pasupathy Arumugam

Dr Pasupathy Arumugam

Consultant Pathologist · Reg: 21521

Last reviewed: September 7, 2026

Overview

To diagnose genetic causes of neurological and neuromuscular diseases, enable early intervention, assess risk for family members, and guide personalized treatment strategies.

Test Code
2976
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

Common Neurological/neuromuscular diseases 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.

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: 4-6 weeks

Patient Instructions

1
Before the Test:Obtain a doctor's prescription if required; no fasting needed; inform about any medications or conditions.
2
During the Test:Sample collection via blood draw or other specified methods; minimal discomfort.
3
After the Test:Resume normal activities; await results within 4-6 weeks.

About This Test

Who Should Get This Test

To diagnose genetic causes of neurological and neuromuscular diseases, enable early intervention, assess risk for family members, and guide personalized treatment strategies.

How to Prepare

  • Collect peripheral blood in EDTA Vacutainer
  • For amniotic fluid or chorionic villi, use sterile containers
  • Ensure proper labeling and transport with cool pack

Doctor's Notes

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

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeAmniotic fluid, Chorionic villi, Peripheral blood
ContainerSterile container, Sterile Normal Saline Container, EDTA Vacutainer

Understanding Your Results

Results indicate the presence or absence of genetic mutations associated with neurological and neuromuscular diseases.
Positive result: Pathogenic mutation detected, indicating increased risk or diagnosis; consult a genetic counselor or specialist.
Negative result: No pathogenic variants found; clinical correlation with symptoms is recommended.
Variant of uncertain significance (VUS): Further testing or family studies may be needed.
Results should be interpreted in conjunction with clinical history and other diagnostic tests.
⚠️ When to Consult a Doctor:

If you experience symptoms such as weakness, tremors, memory loss, or have a family history of neurological diseases, consult a healthcare professional for evaluation and to discuss testing options.

Frequently Asked Questions

What is the Common Neurological/Neuromuscular Diseases Gene Panel?
It is a DNA test that analyzes genes associated with neurological and neuromuscular disorders to identify genetic mutations.
What conditions does this panel test for?
It covers conditions like Alzheimer's disease, Parkinson's disease, muscular dystrophy, multiple sclerosis, and other related disorders.
Who should consider this test?
Individuals with symptoms such as weakness, tremors, memory loss, or a family history of these diseases.
How is the test performed?
A sample of peripheral blood, amniotic fluid, or chorionic villi is collected and analyzed using Next-Generation Sequencing (NGS).
What is the cost of the test?
The test costs INR 36000, which includes sample collection, analysis, and report generation.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across many cities in India.
How long does it take to get results?
Results are typically available within 4-6 weeks after sample collection.
Is the test covered by insurance?
Yes, it is covered by most insurance plans, but coverage may vary; check with your provider.
What are the symptoms of neurological diseases?
Common symptoms include weakness, numbness, tremors, difficulty speaking, memory loss, balance issues, and chronic pain.
How accurate is the gene panel test?
The test uses advanced NGS technology for high accuracy, but results should be interpreted by a healthcare professional.
Do I need a doctor's prescription for this test?
Yes, a doctor's prescription is generally required, except for surgery, pregnancy, or travel abroad cases.
What should I do after receiving the test results?
Consult a healthcare professional or genetic counselor to understand the results and discuss next steps.
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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