Angelman-like Syndrome

Sponsored diagnostic testing programs for Angelman-like Syndrome

Angelman-like syndrome refers to a group of neurogenetic conditions that share features with Angelman syndrome—such as developmental delay, limited speech, seizures, and characteristic movement or behavioral patterns—but arise from different genetic causes. Genetic testing helps clarify the underlying diagnosis and guide clinical management and counseling.

1 program found for Angelman-like Syndrome

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