Epilepsy is a neurological disorder characterized by recurring seizures. It can be caused by injuries, illnesses, genetics, or unknown causes. It is usually diagnosed after two or more unprovoked seizures, with symptoms such as jerky movements, confusion, muscle stiffness, fear, or anxiety that are unexplained.
As a comprehensive panel that includes all the genes found in the Neonatal, Childhood, Adolescent/Adult, and PME Epilepsy Panels, this panel encompasses a wide range of genes associated with seizure activity.

What kind of person should consider this test?

If a patient has a personal or family history of epilepsy and seizures, this panel may be recommended.

What are the potential advantages for my patient?

Identifying the pathogenetic variant responsible for inherited epilepsy and pinpointing the cause can be achieved with genetic testing. Epilepsy genetic testing can provide useful information for managing and preventing seizures and related health problems.

• Explain the potential progression of the disease over time.

• Help family members understand their own health risks.

• Offer tailored treatment plans and symptom management strategies.

• Provide options and guidance for family planning.

• Confirm or determine the accurate diagnosis.

• Identify possible complications or related symptoms.

• Connect patients with useful resources and support networks.