Minimal encephalopathy in hereditary hemorrhagic telangiectasia patients with portosystemic vascular malformations
HHT patients with PSM showed higher attention difficulties than HHT controls, though both PSM and HHT controls showed findings of mHE. Specific neuropsychological tests for early detection of mHE should be considered in HHT patients.
Authors
- Ana Isabel Cañabate
- José Castellote (ORCID: https://orcid.org/0000-0002-8528-3112)
- Antoni Riera‐Mestre (ORCID: https://orcid.org/0000-0001-9411-804X)
- Adriana Iriarte (ORCID: https://orcid.org/0000-0002-7708-368X)
- Esther Alba
- Enric Gamundí (ORCID: https://orcid.org/0000-0001-5871-5330)
- Xavier Pintó (ORCID: https://orcid.org/0000-0002-2216-2444)
- Q. Ordi
- Pau Cerdà (ORCID: https://orcid.org/0000-0003-4368-6260)
- Jesús Ribas (ORCID: https://orcid.org/0000-0001-7356-4307)
- Raquel Torres-Iglesias (ORCID: https://orcid.org/0000-0001-9204-9888)
- B. Villanueva (ORCID: https://orcid.org/0009-0009-4004-4706)
- L. A. Sanz-Astier
Institutions
- Instituto de Salud Carlos III (ES)
- Spanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition (ES)
- Bellvitge University Hospital (ES)
- Institut d'Investigació Biomédica de Bellvitge (ES)
- Hospital Universitario Son Espases (ES)
- Universitat de Barcelona (ES)
Publication Details
- Journal
- Orphanet Journal of Rare Diseases
- Published
- 2024-12-21
- DOI
- https://doi.org/10.1186/s13023-024-03493-3
- Citations
- 2
- Primary Topic
- Vascular Anomalies and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.88
Funders
- Centres de Recerca de Catalunya
- Generalitat de Catalunya
- Instituto de Salud Carlos III
- European Regional Development Fund