Seizure Disorder,Childhood Absence Epilepsy,Hyperprolinemia,Cerebral Creatine Deficiency Syndrome 2,Aromatic L-Amino Acid Decarboxylase Deficiency,Riboflavin Deficiency,Molybdenum Cofactor Deficiency,Sulfite Oxidase Deficiency, Isolated,Multiple Carboxylase Deficiency,Early Myoclonic Encephalopathy,Encephalopathy,Hypophosphatasia,Benign Neonatal Seizures,Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency,West Syndrome,Acid-Labile Subunit Deficiency,Hyperprolinemia, Type Ii,Hypophosphatasia, Infantile,Glycine Encephalopathy,Neonatal Period Electroclinical Syndrome,Infancy Electroclinical Syndrome,Early Infantile Epileptic Encephalopathy,Vitamin Metabolic Disorder,Cerebral Creatine Deficiency Syndrome,Dravet Syndrome,Biotinidase Deficiency,Holocarboxylase Synthetase Deficiency,Epilepsy, Myoclonic Juvenile,Autosomal Dominant Nocturnal Frontal Lobe Epilepsy,Neuronopathy, Distal Hereditary Motor, Type Va