Hereditary renal amyloidosis with a variant lysozyme p.Trp82Arg in a Chinese family: case report and literature review

BACKGROUND: Lysozyme amyloidosis is a rare hereditary systemic amyloidosis with amyloid deposits in various tissues leading to progressive organ failure. It has been mainly reported in developed countries since 1993. Here we report a lysozyme amyloidosis family with variant lysozyme p.Trp82Arg in a...

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Detalles Bibliográficos
Autores principales: Li, Zhenyu, Xu, Hui, Liu, Dan, Li, Danyang, Liu, Gang, Wang, Su-xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686406/
https://www.ncbi.nlm.nih.gov/pubmed/31395023
http://dx.doi.org/10.1186/s12882-019-1496-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686406/
https://www.ncbi.nlm.nih.gov/pubmed/31395023
http://dx.doi.org/10.1186/s12882-019-1496-6

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