Sponsored diagnostic testing programs for Christianson Syndrome
Christianson syndrome is a rare X-linked neurodevelopmental disorder caused by variants in the SLC9A6 gene. It is characterized by global developmental delay, seizures, impaired speech, ataxia, and features that may resemble Angelman syndrome. Genetic testing confirms the diagnosis and helps guide care planning and family counseling.
1 program found for Christianson Syndrome
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.
