Hereditary transthyretin amyloidosis: a case report

BACKGROUND: Hereditary transthyretin amyloidosis is an uncommon multisystem disorder caused by mutation of the transthyretin protein, leading to peripheral neuropathy often with autonomic features, cardiomyopathy, or a mixed phenotype. Multiple other organ systems can be involved with ophthalmologic...

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Detalles Bibliográficos
Autores principales: Lee, Angela, Fine, Nowell M., Bril, Vera, Delgado, Diego, Hahn, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233400/
https://www.ncbi.nlm.nih.gov/pubmed/35751086
http://dx.doi.org/10.1186/s13256-022-03437-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233400/
https://www.ncbi.nlm.nih.gov/pubmed/35751086
http://dx.doi.org/10.1186/s13256-022-03437-0

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