GM3 Synthase Deficiency

Sponsored diagnostic testing programs for GM3 Synthase Deficiency

GM3 synthase deficiency is a rare neurodevelopmental disorder caused by impaired ganglioside synthesis, leading to severe developmental delay, hypotonia, seizures, and often visual or hearing impairment. Many children have failure to achieve independent ambulation or speech. Genetic testing confirms the diagnosis and informs supportive care and counseling.

1 program found for GM3 Synthase 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