Diagnostic delay in patients with sporadic hereditary transthyretin-mediated amyloidosis
There is an important diagnostic delay in sporadic cases of ATTRv amyloidosis. Awareness should be spread among clinicians regarding the various manifestations of this disease, stressing the importance of family history and epidemiological data.
Authors
- B.P. Antunes
- Mamede de Carvalho (ORCID: https://orcid.org/0000-0001-7556-0158)
- Isabel M. Conceição (ORCID: https://orcid.org/0000-0003-0934-9631)
- Catarina Falcão de Campos (ORCID: https://orcid.org/0000-0001-6194-9787)
Institutions
- University of Lisbon (PT)
- Hospital de Santa Maria (PT)
Publication Details
- Journal
- Neurological Sciences
- Published
- 2024-10-10
- DOI
- https://doi.org/10.1007/s10072-024-07793-1
- Citations
- 1
- Primary Topic
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 0.23
Funders
- Universidade de Lisboa
- Fundação para a Ciência e a Tecnologia