C9ORF72 hexanucleotide repeat expansion with Alzheimer's disease-like clinical phenotype: A case report with results from neuropsychology, CSF, FDG-PET, and PiB-PET
Research output: Contribution to journal › Journal article › Research › peer-review
Documents
- C9ORF72 hexanucleotide repeat expansion with Alzheimer's disease‐like clinical phenotype: A case report with results from neuropsychology, CSF, FDG‐PET, and PiB‐PET
Final published version, 382 KB, PDF document
A thorough family history and relevant investigation program are essential to settle accurate diagnosis when clinical presentation is atypical or with a mixed picture.
| Original language | English |
|---|---|
| Journal | Clinical Case Reports |
| Volume | 8 |
| Issue number | 12 |
| Pages (from-to) | 3416-3420 |
| ISSN | 2050-0904 |
| DOIs | |
| Publication status | Published - 2020 |
- Alzheimer's disease, C9Orf72 gene mutation, frontotemporal dementia, genetic testing
Research areas
Number of downloads are based on statistics from Google Scholar and www.ku.dk
No data available
ID: 251943483