Leigh Syndrome Due to Mitochondrial Complex IV Deficiency

Sponsored diagnostic testing programs for Leigh Syndrome Due to Mitochondrial Complex IV Deficiency

Leigh syndrome due to complex IV deficiency is a mitochondrial disorder presenting with progressive neurologic decline, hypotonia, feeding problems, seizures, and characteristic brain lesions. Onset is typically in infancy. Genetic testing confirms the diagnosis and guides metabolic management and counseling.

1 program found for Leigh Syndrome Due to Mitochondrial Complex IV 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
ViewOrder
Performing labInvitae | Labcorp