Neuropediatrics, Inhaltsverzeichnis Neuropediatrics 2022; 53(03): 217DOI: 10.1055/s-0042-1744159 Videos and Images in Neuropediatrics Atypical Hemifacial Spasm and Myoclonus Related to AIFM1 Variant Authors Institutsangaben Frédérique Depierreux 1 Department of Neurology, Centre Hospitalier Universitaire, CHU, Liège, Belgium Serpil Alkan 2 Department of Pediatrics, Centre Hospitalier Universitaire, CHU, Liège, Belgium Artikel empfehlen Abstract Artikel einzeln kaufen(opens in new window) Volltext Referenzen References 1 Pandolfo M, Rai M, Remiche G, Desmyter L, Vandernoot I. Cerebellar ataxia, neuropathy, hearing loss, and intellectual disability due to AIFM1 mutation. Neurol Genet 2020; 6 (03) e420 2 Heimer G, Eyal E, Zhu X. et al. Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin. Eur J Paediatr Neurol 2018; 22 (01) 93-101 3 Yaltho TC, Jankovic J. The many faces of hemifacial spasm: differential diagnosis of unilateral facial spasms. Mov Disord 2011; 26 (09) 1582-1592
