Atypical AD with mixed logopenic / non‐fluent primary progressive aphasia and ANXA11 gene mutation: a case report
This report can provide valuable insight into considering AD when confronted with atypical clinical presentations with mixed-PPA, as in this case. It also reinforces the clinical variability of ANXA11 gene mutations and highlights the importance of using DTI for detecting WM matter-specific pattern changes in different PPA phenotypes.
Authors
- Rairis Barbosa Nascimento
- Gustavo Dalul Gomez (ORCID: https://orcid.org/0000-0003-4321-0545)
- Correia Marin
- Camila Farias de Araujo (ORCID: https://orcid.org/0000-0002-8359-3846)
- Alan Cronemberger Andrade (ORCID: https://orcid.org/0000-0003-1645-0500)
- Paulo Henrique Ferreira Bertolucci (ORCID: https://orcid.org/0000-0001-7902-7502)
- Paulo Eduardo Lahoz Fernandez
- Marcelo dos Santos Bandeira Filho
- Sheilla de Medeiros
Institutions
- Universidade Federal de São Paulo (BR)
Publication Details
- Journal
- Alzheimer s & Dementia
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1002/alz70857_101641
- Primary Topic
- Neurobiology of Language and Bilingualism
- Type
- article
- Field-Weighted Citation Impact
- 0.00