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• W2008771350 abstract "The hexanucleotide repeat in the chromosome 9 open reading frame 72 (C9ORF72) gene was recently discovered as the underlying genetic cause of many families with frontotemporal dementia (FTD) and/or amyotrophic lateral sclerosis (ALS) linked to chromosome 9 (c9FTD/ALS). We report the clinical, neuropsychologic, and neuroimaging findings of a family with the C9ORF72 mutation and clinical diagnoses bridging the FTD, parkinsonism, and ALS spectrum.To characterize the antemortem characteristics of a family with c9FTD/ALS associated with the GGGGCC repeat expansion in C9ORF72.Clinical series.Tertiary care academic medical center. PATIENTS The members of a family affected by the mutation with features of FTD and/or ALS.Clinical, neuropsychologic, and neuroimaging assessments.All 3 examined subjects had the hexanucleotide expansion detected in C9ORF72. All had personality/behavioral changes early in the course of the disease. One case had levodopa-unresponsive parkinsonism, and 1 had ALS. Magnetic resonance imaging showed symmetric bilateral frontal, temporal, insular, and cingulate atrophy.This report highlights the clinical and neuroimaging characteristics of a family with c9FTD/ALS. Further studies are needed to better understand the phenotypical variability and the cliniconeuroimaging-neuropathologic correlations." @default.
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• W2008771350 date "2012-09-01" @default.
• W2008771350 modified "2023-09-26" @default.
• W2008771350 title "Characterization of a Family With c9FTD/ALS Associated With the GGGGCC Repeat Expansion in C9ORF72" @default.
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• W2008771350 doi "https://doi.org/10.1001/archneurol.2012.772" @default.
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