Multigene Panel Analysis for Neuromuscular Disorders
This test examines genetic variations linked to neuromuscular conditions, helping identify potential causes of muscle weakness, nerve damage, or movement disorders.
["This test checks for genetic mutations that may affect how your muscles and nerves function."]
Key facts at a glance
- LOINC
- 103957-7
- Short code
- Neuromuscular multigene analysis Spec
- Synonyms
- Neuromuscular multigene analysis Spec
- Category
- chemistry
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- molgen
- CPT
- 86038
- Specimen volume
- 5 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 4–24 hours
- Order
- routine
What Does This Test Measure?
The test analyzes multiple genes associated with neuromuscular diseases, including those that may cause conditions like muscular dystrophy, peripheral neuropathy, or congenital myopathies. It looks for specific genetic changes (mutations) that could influence muscle or nerve function.
Why Might This Test Be Ordered?
Your healthcare provider may recommend this test if you have symptoms like muscle weakness, fatigue, difficulty moving, or a family history of neuromuscular disorders. It can also be used for genetic counseling or prenatal screening in certain cases.
How Is the Sample Collected?
A blood sample is typically taken from a vein in your arm. This is the most common specimen type for genetic testing, as it provides enough DNA for analysis.
What Are the Possible Outcomes?
Results may include: (1) No significant genetic changes found, (2) A likely pathogenic mutation identified, or (3) Variants of uncertain significance detected. Follow-up testing or genetic counseling may be recommended based on findings.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Clinical Significance: This test plays a critical role in diagnosing neuromuscular disorders by identifying genetic causes that may not be apparent through traditional medical testing. Early detection can influence treatment options, family planning, and long-term management strategies.
Short name
Neuromuscular Gene Testing
Frequently asked questions
How long does it take to get results from this test?
What if my test results show a genetic mutation linked to a neuromuscular disorder?
Can this test be used for prenatal or newborn screening?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy