Skip to main content
DNA Labs India

Muscular Dystrophy Gene Panel Test

DNA Labs India | ISO 9001:2015 Certified

Muscular Dystrophy Gene Panel Test

Short Name: Muscular Dystrophy Panel

Also known as: MD Gene Panel, Muscular Dystrophy Genetic Test

Muscular Dystrophy Gene Panel Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood samples. Results in 4-5 weeks. Free home collection in 300+ cities across India.

Genetic TestAll Ages🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

To diagnose muscular dystrophy by identifying specific genetic mutations, guide treatment decisions, facilitate genetic counseling, and enable personalized management for patients and families.

Test Code
3101
Price
₹20,000
Sample Type
Blood
Result Time
4-5 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation required. A doctor's prescription may be needed, except for surgery, pregnancy, or travel abroad cases.

Method: Venipuncture

Step 2

Laboratory Analysis

Blood sample collected via venipuncture into an EDTA tube or onto an FTA card by a trained phlebotomist.

Step 3

Report Delivery

Sample is labeled, stored appropriately, and transported to the laboratory for genetic analysis.

Timeline: 4-5 weeks

Patient Instructions

1
Before the Test:No specific preparation required. Doctor's prescription may be needed.
2
During the Test:Blood sample collected via venipuncture; procedure takes about 10-15 minutes.
3
After the Test:Sample sent to lab; results available in 4-5 weeks. Mild bruising at collection site may occur.

About This Test

Who Should Get This Test

To diagnose muscular dystrophy by identifying specific genetic mutations, guide treatment decisions, facilitate genetic counseling, and enable personalized management for patients and families.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection equipment
  • Label sample correctly with patient details
  • Follow standard phlebotomy procedures

Doctor's Notes

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

"This gene panel is crucial for accurate diagnosis and personalized treatment planning for muscular dystrophy patients, enabling targeted management and genetic counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood
Sample Volume3 ml
ContainerEDTA tube and FTA Card
Collection MethodVenipuncture

Sample Stability

Blood in EDTA tube: Stable for 48 hours at room temperature
Blood on FTA card: Stable for extended periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted sample
  • Insufficient sample volume
  • Improper labeling or identification
  • Contaminated sample

Understanding Your Results

Results indicate the presence or absence of genetic mutations associated with muscular dystrophy, aiding in diagnosis and management.
📊

Positive (Pathogenic variant detected)

Confirms diagnosis of muscular dystrophy; specific type identified based on gene mutation. Recommend genetic counseling and tailored treatment.

📊

Negative (No pathogenic variants detected)

No known mutations found; clinical correlation advised. Consider other diagnostic tests if symptoms persist.

⚠️ When to Consult a Doctor:

Consult a doctor if symptoms of muscular dystrophy are present, for genetic counseling after test results, or if there is a family history of the condition.

Limitations

  • ⚠May not detect all mutations, including novel or rare variants
  • ⚠Does not assess for other genetic or non-genetic conditions
  • ⚠Results require clinical correlation and genetic counseling

Risks & Considerations

  • ●Minor bruising or pain at blood draw site
  • ●Rare risk of infection or fainting
  • ●Emotional impact of genetic results

Interfering Factors

  • ●Sample contamination
  • ●Improper sample storage or handling
  • ●DNA degradation due to delays in processing

Compare With Similar Tests

TestMuscular Dystrophy Gene PanelCreatine Kinase (CK) TestMuscle Biopsy
ComparisonMuscular Dystrophy Gene PanelCK test measures muscle damage via blood enzyme levels, while the gene panel identifies the underlying genetic cause for precise diagnosis.Muscle biopsy examines muscle tissue histologically, whereas the gene panel provides non-invasive genetic analysis for mutation detection.

Frequently Asked Questions

What is the Muscular Dystrophy Gene Panel Test?
It is a genetic test that analyzes multiple genes to identify mutations causing various types of muscular dystrophy, aiding in accurate diagnosis.
How much does the Muscular Dystrophy Gene Panel Test cost in India?
The test costs INR 20,000 at DNA Labs India, with free home sample collection available across many cities.
What types of muscular dystrophy does this test detect?
It detects Duchenne, Becker, limb-girdle, facioscapulohumeral, and other forms based on gene mutations analyzed.
How is the test performed?
A blood sample is collected via venipuncture and analyzed using Next-Generation Sequencing (NGS) technology in the lab.
Is fasting required for this test?
No, fasting is not required. The test can be done at any time with a blood sample.
How long does it take to get results?
Results are typically available within 4-5 weeks after sample collection.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in numerous cities across India.
What should I do if I have a family history of muscular dystrophy?
Consult a doctor or geneticist to discuss testing options, including this gene panel, for early diagnosis and counseling.
Can this test be used for prenatal diagnosis?
This test is primarily for postnatal diagnosis; prenatal testing may require different methods like chorionic villus sampling.
What are the symptoms of muscular dystrophy?
Common symptoms include progressive muscle weakness, loss of muscle mass, difficulty walking, and delayed motor skills in children.
How accurate is this test?
The test is highly accurate for detecting known pathogenic mutations, but may not identify all rare variants; clinical correlation is advised.
Do I need a doctor's prescription for this test?
Yes, a doctor's prescription is generally required, except for cases involving surgery, pregnancy, or travel abroad.
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

Angelman Syndrome Test

₹10,000

Duchenne / Becker Muscular Dystrophy (DMD / BMD) Gene Mutation Test

₹14,000

Episodic Ataxia Type 1 Hotspot Test

₹11,500

Episodic Ataxia Comprehensive Profile Hotspot Test

₹16,000

Megalencephalic Leukoencephalopathy with Subcortical Cysts Van Der Knaap and Nalband MLC Gene Hotspot Mutation Test

₹7,500

Analyzer 18 SMA 18 Test Panel

₹1,755
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.