Cortical dysplasia-focal epilepsy syndrome is an autosomal recessive disorder characterized primarily by cortical dysplasia, intractable focal seizures, relative macrocephaly and diminished deep-tendon reflexes. A homozygous single-base deletion, c.3709delG (p.Asp1237Ilefs*17) in exon 22 of the CNTNAP2 gene was identified as the genetic cause of this disorder in a large group of Old Order Amish patients. This targeted test will specifically analyze the c.3709delG pathogenic variant.
Type B
1 - 2 weeks