Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series - Dzinovic, Ivana; Škorvánek, Matej; Necpál, Ján; Boesch, Sylvia; Švantnerová, Jana; Wagner, Matias; Havránková, Petra; Pavelekova, Petra; Haň, Vladimír; Janzarik, Wibke G.; Berweck, Steffen; Diebold, Isabel; et al. (Parkinsonism & related disorders, 2021)
Keywords: Adolescent; Brain Diseases - complications; Brain Diseases - genetics; Child; Child, Preschool; Dystonia; Dystonia - genetics; Epilepsy; Epilepsy-dyskinesia spectrum; Epileptic Syndromes - complications; Epileptic Syndromes - genetics; Female; Forkhead Transcription Factors - genetics; GTP-Binding Protein alpha Subunits, Gi-Go - genetics; Humans; Life Sciences; Male; Methyl-CpG-Binding Protein 2 - genetics; Nerve Tissue Proteins - genetics; Neurodevelopmental disease; Neurodevelopmental Disorders - complications; Neurodevelopmental Disorders - genetics; Phenotype; Receptors, GABA-A - genetics; Receptors, GABA-B - genetics; Epilepsy-dyskinesia spectrum; Neurodevelopmental disease; Dystonia; Epilepsy