Myoclonic Epilepsy with Ataxia

Sponsored diagnostic testing programs for Myoclonic Epilepsy with Ataxia

Myoclonic epilepsy with ataxia is characterized by myoclonic seizures, gait unsteadiness, and impaired coordination, often beginning in childhood or adolescence. Cognitive function may be normal or mildly affected depending on the underlying cause. Genetic testing clarifies etiology and helps guide management and family counseling.

1 program found for Myoclonic Epilepsy with Ataxia

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