Co-existence of Alport syndrome and C3 glomerulonephritis in a proband with family history

BACKGROUND: Alport syndrome and C3 glomerulonephritis (C3GN) are rare kidney diseases, frequently responsible for familial haematuria, proteinuria, and renal impairment. With the rapid development of molecular genetic testing, Alport syndrome causes have been restricted mostly to variants in the COL...

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Detalles Bibliográficos
Autores principales: Ding, Yin, Tang, Xuanli, Du, Yuanyuan, Chen, Hongyu, Yu, Dongrong, Zhu, Bin, Yuan, Bohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265006/
https://www.ncbi.nlm.nih.gov/pubmed/34238373
http://dx.doi.org/10.1186/s40001-021-00543-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265006/
https://www.ncbi.nlm.nih.gov/pubmed/34238373
http://dx.doi.org/10.1186/s40001-021-00543-5

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