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Background: Fahr's syndrome is a rare neurological disorder, mostly marked by idiopathic calcification of the basal ganglia, often inherited in an autosomal dominant manner.[1] Motor symptoms are one of the most common manifestations, such as movement disorder (e.g., parkinsonism, dystonia, ataxia, chorea).[2] Non‐motor symptoms, such as cognitive decline or psychiatric disturbances, though their impact on quality of life, are frequently undervalued in these cases