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      Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

      Neurology
      Aged, Atrophy, Brain, pathology, Brain Diseases, complications, diagnosis, Fragile X Mental Retardation Protein, Fragile X Syndrome, genetics, metabolism, Heterozygote, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Motivation, Nerve Tissue Proteins, Parkinsonian Disorders, RNA, Messenger, RNA-Binding Proteins, Tremor

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          Abstract

          The authors report five elderly men with the fragile X premutation who had a progressive action tremor associated with executive function deficits and generalized brain atrophy. These individuals had elevated fragile X mental retardation 1 gene (FMR1) messenger RNA and normal or borderline levels of FMR1 protein. The authors propose that elevations of FMR1 messenger RNA may be causative for a neurodegenerative syndrome in a subgroup of elderly men with the FMR1 premutation.

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