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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]