Cost 
$2,000.00
TAT 
8 weeks
CPT Code 
81407
Test Code 
3121
Test Methods 
Sequencing
Specimen Types Accepted 
Blood
Saliva
Cultured Cells
Extracted DNA
Notes 
If no pathogenic sequence changes are identified in this panel, we are able to reflex to analysis of selected panels related to neuromuscular disease at no additional charge. Please contact one of our genetic counselors for more information.

Bethlem myopathy (BM) is a variable autosomal dominant condition, associated with proximal muscle weakness and variable contractures. Onset ranges from the prenatal period to adulthood

Ullrich congenital muscular dystrophy  (UCMD) is an autosomal recessive condition associated with congenital weakness, hypotonia, joint contractures, and hyperlaxity of distal joints