Cost 
$3,500.00
TAT 
8 weeks
CPT Code 
81406
81407
Test Code 
1127
Test Methods 
Sequencing
Deletion/Duplication analysis
Specimen Types Accepted 
Blood
Saliva
Buccal
Cultured Cells
Extracted DNA
Notes 
Any gene in the Cerebral Cortical Malformations Panel can also be ordered individually. Please contact us directly for cost and CPT code information.

Cerebral cortical malformations include a diverse group of developmental disorders that are common causes of neurodevelopmental delay and epilepsy.  These disorders include lissencephaly, pachygyria, polymicrogyria and microcephaly. Numerous genes are associated with malformations of cortical developmental, which might disrupt each of the main stages of cell proliferation and specification, neuronal migration and late cortical organization. The disruption of these steps produces characteristic morphologic anomalies, typically abnormal sulcation and gyral patterns.

Our Cerebral Cortical Malformation Sequencing Panel includes sequence analysis of the following 46 genes: ACTB, ACTG1, ARFGEF2, ARX, ATP6V0A2, B3GALNT2, B3GNT1, DCX, DYNC1H1, ERMARD, FKRP, FKTN, GMPPB, GPR56, KIAA1279, KIF2A, KIF5C, LAMA2, LAMC3, LARGE, NDE1, OCLN, PAFAH1B1 (LIS1), POMGNT1, POMGNT2, POMK, POMT1, POMT2, RAB18, RAB3GAP1, RAB3GAP2, RELN, RTTN, SNAP29, SRD5A3, TBC1D20, TUBA1A, TUBA8, TUBB, TUBB2A, TUBB2B, TUBB3, TUBB4A, TUBG1, VLDLR, WDR62.

Any gene in the Cerebral Cortical Malformation Sequencing Panel can also be ordered individually. Please contact us directly for cost and CPT code information.