autism spectrum disorder genetic testing

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodesĭiabetes-deafness syndrome, Mitochondrial myopathy, infantile, transient, Mitochondrial myopathy with diabetes Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, Oncocytoma, Leber hereditary optic neuropathy, Leber optic atrophy and dystonia, Mitochondrial complex I deficiency Myoclonic epilepsy with ragged red fibers, Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, Leber hereditary optic neuropathy, Mitochondrial complex I deficiency Leber hereditary optic neuropathy, Leber optic atrophy and dystonia, Mitochondrial complex I deficiency Leber optic atrophy and dystonia, Mitochondrial complex I deficiency Leber hereditary optic neuropathy, Mitochondrial complex I deficiency Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, Leber hereditary optic neuropathy, Leber optic atrophy and dystonia Myoglobinuria, recurrent, Leber hereditary optic neuropathy, Sideroblastic anemia, Cytochrome C oxidase deficiency, Deafness, mitochondrialĬytochrome c oxidase deficiency, Leber hereditary optic neuropathy Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Ataxia and polyneuropathy, adult-onset, Cardiomyopathy, infantile hypertrophic, Leigh syndrome, Striatonigral degeneration, infantile, mitochondrialĬardiomyopathy, apical hypertrophic, and neuropathy, Cardiomyopathy, infantile hypertrophic Mental retardation, autosomal recessive 57Īngelman-like syndrome, Autism, Rett syndrome, Encephalopathy, Intellectual developmental disorder Guanidinoacetate methyltransferase deficiencyĭevelopmental delay and seizures with or without movement abnormalities (DEDSM), Autism spectrum disorder, overgrowth syndrome with intellectual disability Mental retardation with language impairment and autistic features, Congenital heart malformations Mental retardation, autosomal dominant 34 Mental retardation, autosomal recessive 3 Helsmoortel-van der Aa syndrome (Mental retardation, autosomal dominant 28)ĭevelopmental delay and seizures with or without movement abnormalities (DEDSM)īrugada syndrome, Timothy syndrome, Neurodevelopmental disorder

Autism spectrum disorder genetic testing