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• W2170622311 abstract "Frontotemporal degeneration (FTD) and amyotrophic lateral sclerosis (ALS) are related but distinct neurodegenerative diseases. The identification of a hexanucleotide repeat expansion in a noncoding region of the chromosome 9 open reading frame 72 (C9ORF72) gene as a common cause of FTD/ALS, familial FTD, and familial ALS marks the culmination of many years of investigation. This confirms the linkage of disease to chromosome 9 in large, multigenerational families with FTD and ALS, and it promotes deeper understanding of the diseases' shared molecular FTLD-TDP pathology. The discovery of the C9ORF72 repeat expansion has significant implications not only for familial FTD and ALS, but also for sporadic disease. Clinical and pathological correlates of the repeat expansion are being reported but remain to be refined, and a genetic test to detect the expansion has only recently become clinically available. Consequently, individuals and their families who are considering genetic testing for the C9ORF72 expansion should receive genetic counseling to discuss the risks, benefits, and limitations of testing. The following review aims to describe genetic counseling considerations for individuals at risk for a C9ORF72 repeat expansion." @default.
• W2170622311 created "2016-06-24" @default.
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• W2170622311 date "2012-01-01" @default.
• W2170622311 modified "2023-10-14" @default.
• W2170622311 title "Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion" @default.
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• W2170622311 doi "https://doi.org/10.1186/alzrt130" @default.
• W2170622311 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3506941" @default.
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