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Genetic testing for the following syndromes (if your child has certain dysmorphic features or characteristics): Tuberous Sclerosis Complex, Angelman, PraderWilli, Velocardiofacial, and Smith-Lemli-Opitz syndromes Testing for Mitochondrial Dysfunction and Cerebral Folate Deficiency, metabolic disorders with a high prevalence among individuals with ASD and seizures If supporting clinical characteristics exist, consider testing for other, much more rare metabolic disorders, such as: Succinic Semialdehyde Dehydrogenase Deficiency, Adenylosuccinate lyase deficiency, Creatine Metabolism Disorder, Phenylketonuria, Pyridoxine dependent and responsive seizures, and Urea Cycle Disorders Treatment Options for Seizures Seizures are most commonly treated with anti-epileptic drugs (AEDs), but non-AED treatments are also available
Cacciatore I, Cornacchia C, Pinnen F, Mollica A, Di Stefano A
With respect to outcomes, a paucity of evidence highlighted the absence of validated biomarkers necessary to show neuroprotection
