Hyperkinesia in a Young Female With Co-Occurring PSEN1 and HTT Mutations: Examining the Relationship Between Early-onset Familial Alzheimer’s and Huntington’s Diseases (P7-3.020)
Using the first reported case of co-occurring PSEN1 and HTT mutations, we illustrate how hyperkinesia complicates the differentiation of early-onset familial Alzheimer’s disease (EOFAD) and Huntington’s disease (HD).
Authors
- Sean Bong Lee (ORCID: https://orcid.org/0000-0001-6211-3498)
- Firas Kaddouh (ORCID: https://orcid.org/0000-0001-9531-4560)
Institutions
- University of Arizona (US)
Publication Details
- Journal
- Neurology
- Published
- 2025-04-07
- DOI
- https://doi.org/10.1212/wnl.0000000000208508
- Primary Topic
- Neurogenetic and Muscular Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00