Late-onset Familial Amyloidotic Polyneuropathy with Bence Jones Proteinuria and Cardiomyopathy

Familial amyloidotic polyneuropathy is a genetically determined disease characterized by deposition of an anomalous transthyretin. A high index of suspicion is needed for this multisymptomatic and lethal disease to be diagnosed. The patient was a 70-year-old male examined due to hypesthesia in the h...

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Detalles Bibliográficos
Autores principales: García de León, Sira Carrasco, González, Amalia Hernández, Alonso, Carmen Orellana, Lobo, Laura Burriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488573/
https://www.ncbi.nlm.nih.gov/pubmed/28694632
http://dx.doi.org/10.4103/jnrp.jnrp_498_16

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488573/
https://www.ncbi.nlm.nih.gov/pubmed/28694632
http://dx.doi.org/10.4103/jnrp.jnrp_498_16

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