Early-Onset of Transthyretin Amyloidosis in a Young Afro-Caribbean Woman With Thr60Ala Mutation

Transthyretin amyloidosis involves the deposition of transthyretin amyloid fibrils in the body. We report an unusual case of a young Afro-Caribbean woman harboring a Thr60Ala mutation who presented with clinical signs of heart failure and polyneuropathy confirmed with genetic testing and results of...

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Bibliografiset tiedot
Julkaisussa:JACC Case Rep
Päätekijät: Keppel, Stormy C., Brannagan, Thomas H., Helmke, Stephen, Santos, Jeffeny De Los, Gonzalez, Leidy J., Fayerman, Raisy, Teruya, Sergio, Maurer, Mathew S.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2020
Aiheet:
Mini-Focus Issue: Cardiomyopathies and Myocarditis
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8299767/
https://ncbi.nlm.nih.gov/pubmed/34317109
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaccas.2020.08.030
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