A mutation in transthyretin gene in a Mexican patient leading to hereditary amyloidosis: a case report
A high index of suspicion is required for diagnosing transthyretin amyloidosis. This case will help raise awareness among physicians regarding the presence of the G67A mutation in Mexican patients and its management.
Authors
- Tarun Dalia (ORCID: https://orcid.org/0000-0002-4115-6189)
- Zubair I. Shah (ORCID: https://orcid.org/0000-0002-3221-3655)
- M. Malik
Institutions
- University of Kansas Medical Center (US)
Publication Details
- Journal
- Journal of Medical Case Reports
- Published
- 2025-08-04
- DOI
- https://doi.org/10.1186/s13256-025-05308-w
- Primary Topic
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 0.00