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Hemidystonia, unilateral limb choreoathetosis, unilateral limb tremor, faciobrachial dystonia, and myoclonus have been reported in the literature. Keywords: Rasmussen's encephalitis; Hemichorea; Movement disorder EN Rasmussen's encephalitis Hemichorea Movement disorder 542 545 4 05/13/22 20220501 NES 220501 Movement disorders in Rasmussen's encephalitis (RE) are rarely described. Hyperkinetic movement disorders except myoclonus3 have been rarely described in RE because the more predominant presentation of seizures overshadows subtle movement disorders; however, a thorough understanding of movement disorders in RE is important because these may be the only presentations of a patient with RE. [Extracted from the article]

Keywords: infantile-onset ascending hereditary spastic paralysis; ALS2 gene; pyramidal; dystonia; oculomotor apraxia EN infantile-onset ascending hereditary spastic paralysis ALS2 gene pyramidal dystonia oculomotor apraxia 118 121 4 01/05/22 20220101 NES 220101 Infantile-onset ascending hereditary spastic paralysis (IAHSP) is a rare autosomal recessive (AR) neurodegenerative disorder which can be associated with mutations in the alsin ( I ALS2 i ) gene located on chromosome 2q33. Pyramidal, dystonia, infantile-onset ascending hereditary spastic paralysis, ALS2 gene, oculomotor apraxia. [Extracted from the article]

Competing Interests: Drs. Madhaw, Kumar, Radhakrishnan, and Shree report no disclosures relevant to the manuscript and no conflicts of interest for this work.