6 weeks
CPT Code 
Test Code 
Test Methods 
Deletion/Duplication analysis
Specimen Types Accepted 
Cultured Cells
Extracted DNA
If sending saliva, 2 kits are required.

Limb girdle muscular dystrophies is a term generally used to describe progessive weakness and wasting restricted to the limb musculature (proximal greater than distal), due to a genetic defect that is distinct from X-linked dystrophinopathy. Muscle biopsy can show diffuse variation in fiber size, necrosis, regeneration and fibrosis. Onset of symptoms can range from early childhood to late adulthood, and  progression and distribution of the weakness and wasting can vary considerably amongst individuals and subtypes.  

Our Limb Girdle Muscular Dystrophy Sequencing Panel includes all of the following 25 genes: MYOT, LMNA, CAV3, DES, DNAJB6, FLNC, CAPN3, DYSF, SGCG, SGCA, SGCB, SGCD, TCAP, TRIM32, FRKP, TTN, POMT1, ANO5, FKTN, POMT2, POMGnT1, DAG1, PLEC, GAA, ISPD.