SCN1A-Related Conditions (Febrile Seizures, Genetic Epilepsy with Febrile Seizures Plus, Dravet Syndrome, Intractable Childhood Epilepsy with Generalized Tonic-Clonic Seizures)

Sponsored diagnostic testing programs for SCN1A-Related Conditions (Febrile Seizures, Genetic Epilepsy with Febrile Seizures Plus, Dravet Syndrome, Intractable Childhood Epilepsy with Generalized Tonic-Clonic Seizures)

SCN1A-related disorders range from mild febrile seizures to severe epileptic encephalopathy such as Dravet syndrome. Developmental impairment and drug-resistant seizures are common in severe forms. Genetic testing confirms the diagnosis and informs treatment decisions and prognosis.

1 program found for SCN1A-Related Conditions (Febrile Seizures, Genetic Epilepsy with Febrile Seizures Plus, Dravet Syndrome, Intractable Childhood Epilepsy with Generalized Tonic-Clonic Seizures)

Programs

1 program
Invitae Unlock™

Invitae Epilepsy Panel

This program provides access to genetic testing for pediatric patients under 18 who present with an unprovoked seizure. The panel evaluates key epilepsy-associated genes to support diagnostic confirmation, inform prognosis, and guide clinical management. Testing is available to eligible patients when ordered by a licensed healthcare provider.

Neurology