PIGG-Congenital Disorder of Glycosylation

Sponsored diagnostic testing programs for PIGG-Congenital Disorder of Glycosylation

PIGG-CDG is a GPI-anchor defect characterized by developmental delay, intellectual disability, hypotonia, and often seizures or behavioral issues. Some individuals have structural brain anomalies or organ involvement. Genetic testing confirms the diagnosis and supports anticipatory care and counseling.

1 program found for PIGG-Congenital Disorder of Glycosylation

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
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Performing labInvitae | Labcorp