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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Detaylı Bibliyografya
Yayımlandı:J Am Soc Nephrol
Asıl Yazarlar: 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.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society of Nephrology 2017
Konular:
Up Front Matters
Online Erişim: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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