Sponsored diagnostic testing programs for CNTNAP2-related Conditions
CNTNAP2-related conditions are a group of neurodevelopmental disorders caused by pathogenic variants in the CNTNAP2 gene. Affected individuals may experience developmental delay, speech and language impairment, autism spectrum features, epilepsy, or movement abnormalities. Genetic testing helps clarify the diagnosis and guide care planning and family counseling.
1 program found for CNTNAP2-related Conditions
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.
