Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique Phenotype

Lysozyme amyloidosis (ALys) is a rare form of hereditary amyloidosis that typically manifests with renal impairment, gastrointestinal (GI) symptoms, and sicca syndrome, whereas cardiac involvement is exceedingly rare and neuropathy has not been reported. Here, we describe a 40-year-old man with rena...

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Detalhes bibliográficos
Publicado no:J Am Soc Nephrol
Main Authors: Nasr, Samih H., Dasari, Surendra, Mills, John R., Theis, Jason D., Zimmermann, Michael T., Fonseca, Rafael, Vrana, Julie A., Lester, Steven J., McLaughlin, Brooke M., Gillespie, Robert, Highsmith, W. Edward, Lee, John J., Dispenzieri, Angela, Kurtin, Paul J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2017
Assuntos:
Up Front Matters
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5280032/
https://ncbi.nlm.nih.gov/pubmed/28049649
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2016090951
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