TBC1D24-Related Conditions (Developmental and Epileptic Encephalopathy, Familial Infantile Myoclonic Epilepsy, Progressive Myoclonic Epilepsy)

Sponsored diagnostic testing programs for TBC1D24-Related Conditions (Developmental and Epileptic Encephalopathy, Familial Infantile Myoclonic Epilepsy, Progressive Myoclonic Epilepsy)

TBC1D24-related conditions include a spectrum of epilepsies ranging from familial infantile myoclonic epilepsy to severe developmental and epileptic encephalopathy and progressive myoclonic epilepsy. Associated features may include hearing loss or developmental delay. Genetic testing clarifies the subtype and guides prognosis and treatment.

1 program found for TBC1D24-Related Conditions (Developmental and Epileptic Encephalopathy, Familial Infantile Myoclonic Epilepsy, Progressive Myoclonic Epilepsy)

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
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Performing labInvitae | Labcorp