Muscle Disorders Panel
NGS panel for inherited muscle disorders; analyzes 122 genes (e.g., DMD, RYR1, TTN, LMNA) to detect pathogenic variants across dystrophy and myopathy spectra.
Accessed through the Roadmap2Rare Sponsored Testing Program•Sponsored by Sanofi•Performed by Revvity Omics, Inc.
Designed to help patients understand the purpose of testing and what to expect.
For patients
What this test and program do
Roadmap2Rare is a complimentary testing program in Canada that helps evaluate rare diseases using genetic and biochemical tests. It’s offered by Revvity Omics in collaboration with Sanofi Canada and is available through your healthcare provider. Your clinician will decide which test is appropriate for you.
Who this may help
Could this be right for you or your family?
- You have signs that suggest a muscle problem, such as muscle weakness, unexplained breathing difficulty, or other symptoms of muscle involvement.
- Your clinician has evidence suggesting a muscle disorder (for example, based on exam or prior testing).
- Not for carrier testing.
What to expect
How the process works
- 1
Choose & order
Your clinician decides if this test fits your situation and submits the order.
- 2
Collect & ship
Provide the sample using the kit and instructions; the clinic or lab ships it to Revvity.
- 3
Get results
Results go to your clinician, who explains what they mean and next steps.
Cost & coverage
Understanding potential costs
If you qualify for this program, the sponsor works with the laboratory to help make testing more affordable. Many patients pay little or no out-of-pocket cost. Your exact cost will depend on your insurance coverage and the specific criteria of the program, and the lab can explain what to expect before your sample is processed.
Quality & privacy
How your sample and information are handled
Testing is performed by Revvity Omics, Inc., a CLIA-certified laboratory (CLIA 39D0673919). Your sample is processed using validated methods and quality controls to support reliable genetic results.
Your health information is handled under privacy and security practices that are intended to align with applicable regulations. For program- and lab-specific details, review the privacy information provided by the laboratory and sponsor.
FAQ
Common questions about this program
What is this program for?
It helps evaluate inherited muscle conditions using a multi-gene DNA test your clinician selects for you.
Who is it for?
People with signs of a muscle disorder, such as muscle weakness, unexplained breathing problems, or other symptoms of muscle involvement.
What does the test look for?
Changes (variants) in many genes linked to muscular dystrophies and myopathies (for example, DMD, RYR1, TTN, LMNA).
How will results help me?
Results can support or rule out certain muscle conditions and guide care, referrals, or additional testing.
How long do results take?
Timing varies; your clinician will tell you what to expect and will share your results.
Does this check if I’m just a carrier?
No. This pathway is meant to evaluate suspected disease, not carrier status.
What sample is needed?
Your care team will advise on the sample type and how it’s collected.
What does it cost?
Testing is complimentary in Canada for eligible patients through Roadmap2Rare.
Who explains the results?
Your clinician receives the report and will review what it means and next steps.
Questions to ask your doctor about Muscle Disorders Panel
- Do you think this test is appropriate for me based on my symptoms and history?
- How could the results of this test change my diagnosis or treatment plan?
- What are the potential limitations of this test that I should understand?
- Should any of my family members also be tested based on my results?
- How will we follow up after the results are available?
Notes
See an issue with this program?