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DNA Labs India

Congenital Myopathy Gene Panel Test

DNA Labs India | ISO 9001:2015 Certified

Congenital Myopathy Gene Panel Test

Also known as: Congenital Myopathy Genetic Panel, CM Gene Panel

Congenital Myopathy 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.

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

🩺 Medically Reviewed By

Overview

The purpose of the Congenital Myopathy Gene Panel test is to diagnose congenital myopathy by identifying genetic mutations. It helps confirm the condition, understand its genetic basis, guide treatment decisions, and facilitate genetic counseling for affected individuals and families.

Test Code
2987
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

A doctor's prescription is required, except for surgery, pregnancy, or travel abroad cases.

Method: Varies based on sample type

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:A doctor's prescription is required, except for surgery, pregnancy, or travel abroad cases.

About This Test

Who Should Get This Test

The purpose of the Congenital Myopathy Gene Panel test is to diagnose congenital myopathy by identifying genetic mutations. It helps confirm the condition, understand its genetic basis, guide treatment decisions, and facilitate genetic counseling for affected individuals and families.

How to Prepare

  • Use sterile containers for sample collection
  • Follow standard procedures for blood draw, amniocentesis, or chorionic villi sampling

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
Collection MethodVaries based on sample type

Understanding Your Results

Results of the Congenital Myopathy Gene Panel test indicate the presence or absence of genetic mutations associated with congenital myopathy.
📊

Mutation Detected

Confirms diagnosis of congenital myopathy; genetic counseling recommended for management and family planning.

📊

No Mutation Detected

Congenital myopathy unlikely based on this panel; further clinical evaluation may be needed to rule out other conditions.

⚠️ When to Consult a Doctor:

If symptoms of muscle weakness, delayed development, or respiratory issues are present, or if there is a family history of congenital myopathy.

Risks & Considerations

  • Minimal risk associated with sample collection
  • Potential psychological impact of results

Frequently Asked Questions

What is Congenital Myopathy?
Congenital myopathy is a rare genetic disorder that affects muscles, causing weakness and wasting, often present at birth or in childhood.
What are the symptoms of Congenital Myopathy?
Common symptoms include muscle weakness, difficulty with motor skills, delayed motor development, joint contractures, and respiratory problems.
How is Congenital Myopathy diagnosed?
Diagnosis involves physical examination, medical history, and genetic testing, such as the Congenital Myopathy Gene Panel test.
What is the Congenital Myopathy Gene Panel test?
It is a comprehensive genetic test that identifies mutations in multiple genes associated with congenital myopathy using next-generation sequencing (NGS).
What genes are included in the panel?
The panel tests for mutations in several genes known to be associated with congenital myopathy, though specific genes may vary based on the panel design.
What sample types are accepted for the test?
Accepted samples include amniotic fluid, chorionic villi, and peripheral blood.
How much does the Congenital Myopathy Gene Panel test cost?
The test costs INR 36000 at DNA Labs India, which includes test kit, sample collection, and laboratory analysis.
Is the test covered by insurance?
Yes, the test is covered by most insurance plans, and financial assistance may be available for eligible individuals.
How long does it take to get results?
Results are typically available in 4-6 weeks after sample collection.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across many cities in India.
Do I need a doctor's prescription for the test?
Yes, a doctor's prescription is required, except for surgery, pregnancy, or travel abroad cases.
What should I do if the test result is positive?
If mutations are detected, consult a genetic counselor or specialist for management, treatment options, and family planning advice.
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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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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