RELN-Related Conditions (Lissencephaly, Autosomal Dominant Lateral Temporal Lobe Epilepsy)

Sponsored diagnostic testing programs for RELN-Related Conditions (Lissencephaly, Autosomal Dominant Lateral Temporal Lobe Epilepsy)

RELN-related disorders range from severe lissencephaly with developmental impairment to mild autosomal dominant lateral temporal epilepsy. Presentation varies widely with the underlying variant. Genetic testing clarifies the diagnosis, informs prognosis, and guides counseling.

1 program found for RELN-Related Conditions (Lissencephaly, Autosomal Dominant Lateral Temporal Lobe 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