PRRT2-Related Conditions (Episodic Kinesigenic Dyskinesia, Benign Familial Infantile Seizures, Familial Infantile Convulsions with Paroxysmal Choreoathetosis)

Sponsored diagnostic testing programs for PRRT2-Related Conditions (Episodic Kinesigenic Dyskinesia, Benign Familial Infantile Seizures, Familial Infantile Convulsions with Paroxysmal Choreoathetosis)

PRRT2-related conditions encompass paroxysmal kinesigenic dyskinesia and benign familial infantile seizures, with some individuals experiencing both episodic movement disorders and seizures. Attacks are brief, often triggered by movement or startle, and neurologic examination between episodes is typically normal. Genetic testing confirms the diagnosis and supports counseling and treatment planning.

1 program found for PRRT2-Related Conditions (Episodic Kinesigenic Dyskinesia, Benign Familial Infantile Seizures, Familial Infantile Convulsions with Paroxysmal Choreoathetosis)

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