Alport syndrome combined with lupus nephritis in a Chinese family: A case report

BACKGROUND: Alport syndrome (ATS) is a rare hereditary disease caused by mutations in genes such as COL4A3, COL4A4, and COL4A5. ATS involves a spectrum of phenotypes ranging from isolated hematuria that is nonprogressive to progressive renal disease with extrarenal abnormalities. Although ATS can be...

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Detalles Bibliográficos
Autores principales: Liu, Hui-Fang, Li, Qing, Peng, You-Qun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223833/
https://www.ncbi.nlm.nih.gov/pubmed/34222438
http://dx.doi.org/10.12998/wjcc.v9.i18.4721

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223833/
https://www.ncbi.nlm.nih.gov/pubmed/34222438
http://dx.doi.org/10.12998/wjcc.v9.i18.4721

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