NEW: Track test progress in real time with our test tracker—now live in your provider portal.

Limb-Girdle Muscular Dystrophy Panel

New York
Approved

Genes

ANO5, BVES, CAPN3, CAV3, DES, DMD, DNAJB6, DOK7, DYSF, FKRP, FKTN, GAA, GMPPB, LMNA, MYOT, PNPLA2, POGLUT1, POMGNT1, POMK, POMT1, POMT2, SGCA, SGCB, SGCD, SGCG, SQSTM1, TCAP, TNPO3, TOR1AIP1, TRAPPC11, TRIM32, TTN, VCP

Conditions

  • Limb-Girdle Muscular Dystrophy (LGMD)
  • Muscular Dystrophy-Dystroglycanopathy (LGMD)
  • Walker–Warburg Syndrome

Clinical Utility

  • Molecular confirmation of a clinical diagnosis
  • Identification of at-risk family members
  • Assist with management/treatment decisions
  • Recurrence risk

Lab Method

  • Next-Gen Sequencing
  • Deletion/Duplication Analysis

Test Code

890

CPT Codes*

81404x2, 81405x2, 81406x2, 81408x2, 81479x3, 81161x1

ABN Required

No

Turnaround Time**

4 weeks

Preferred Specimen

2-5 mL Blood - Lavender Top Tube

Alternative Specimen

Buccal Swabs

*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.

Need something else?

Search More Tests