Creatine Transporter Deficiency

Sponsored diagnostic testing programs for Creatine Transporter Deficiency

Creatine transporter deficiency is an X-linked disorder of brain energy metabolism characterized by global developmental delay, intellectual disability, speech delay, and often seizures or behavioral challenges. Brain MR spectroscopy shows reduced creatine levels. Genetic testing confirms the diagnosis and guides management and family counseling.

1 program found for Creatine Transporter Deficiency

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