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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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| Publicado no: | World J Clin Cases |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8223833/ https://ncbi.nlm.nih.gov/pubmed/34222438 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v9.i18.4721 |
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