Myotonia Panel
New York
Approved
Genes
Conditions
- Periodic paralysis
- Brody Disease
- Hyperekplexia
- Lipodystrophy
- Neuromyotonia
- Paramyotonia Congenita
- Potassium-aggrevated myotonia
- Rippling muscle disease
- Myotonia Congenita
- Myotonic Dystrophy
Clinical Utility
- Molecular confirmation of a clinical diagnosis
- Identification of at-risk family members
- Assist with treatment/ management decisions
- Recurrence risk assessment
Lab Method
- Next-Gen Sequencing
- Deletion/Duplication Analysis
- PCR Fragment Analysis
Test Code
TG82
CPT Codes*
81404x1, 81406x2, 81187x1, 81234x1, 81479x3
ABN Required
No
Turnaround Time**
4 weeks
Preferred Specimen
Alternative Specimen
*The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
**Turnaround times are estimates and begin once the sample(s) begin processing at the GeneDx lab and could be extended in situations outside GeneDx’s control.
Test Documents
Billing
Targeted Variant Testing