EpiSEEK® Focus Epilepsy Panel (76 Genes)Courtagen’s epiSEEK® Focus Epilepsy Panel provides extensive genetic analysis and clinical interpretation of data generated by the complete sequencing of disease associated genes related to early onset epilepsy and seizure disorders. Knowing the genetic basis of a child’s epilepsy is valuable for obtaining a definitive diagnosis, estimating prognosis, determining recurrence risks, and guiding treatment choices. In many cases, the precise genetic diagnosis can be important in therapy selection.
This test includes syndromic and non-sydromic disorders associated with epilepsy such as Angelman, Angelman-like syndromes, Rett, atypical Rett syndromes, Cerebral folate deficiency, Creatine deficiency syndromes, Mowat-Wilson syndrome, West syndrome, Ohtahara syndrome, Early onset epileptic encephalopathy, Idiopathic generalized epilepsy, Benign familial neonatal seizures (BFNS), Familial infantile myoclonic epilepsy (FIME), Juvenile myoclonic epilepsy, Progressive myoclonic epilepsy, Epilepsy with behavioral and learning disorder.
Del/Dup Additional Analysis (76 genes): Additional analysis of exon-sized (and larger) deletion and duplication variants in 76 genes is available as an add-on for both the epiSEEK Focus and epiSEEK Comprehensive panels.
Product Information Sheets:epiSEEK® Focus: Epilepsy and Seizure Disorder Panel (76 genes)
epiSEEK® Focus Panel Gene List
Courtagen's Unmatched Customer Support
Turn Around Time: 4-6 weeks. Results are delivered in weeks, not months.
Online Portal: A secure physician online portal is available for ordering genetic tests and accessing patient reports when completed.
Genetic Counselors: Available to address physician’s questions regarding Courtagen test results. Contact us at firstname.lastname@example.org.