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Conclusion: Latinx patients with AIH are, on average, significantly younger at diagnosis
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Both PD and ALS fulfilled the standard clinical criteria and qualify for the rare Brait–Fahn–Schwartz disease.[1] The ALS‐parkinsonism‐dementia complex of Gaum have a close resemblance except that it is endemic to Pacific island of Gaum, extrapyramidal symptoms appear after symptoms of motor neuron disease and it shows poor response to levodopa therapy
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