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This case report describes a 65-year-old male patient diagnosed with flail arm syndrome, a clinical variant of amyotrophic lateral sclerosis (ALS). The patient presented with symmetric wasting and weakness predominantly in the proximal muscles of both arms, leading to functional impairment of the arms, while mobility and bulbar functions were preserved. Electrophysiological and other tests confirmed ALS. During a two-year follow-up, the weakness progressed distally in the arms and to the lower limbs, while

Author

anon_378668477

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EN