Genotype–phenotype correlations and nephroprotective effects of RAAS inhibition in patients with autosomal recessive Alport syndrome

BACKGROUND: Autosomal recessive Alport syndrome (ARAS) is caused by pathogenic variants in both alleles of either COL4A3 or COL4A4 genes. Reports on ARAS are rare due to small patient numbers and there are no reports on renin-angiotensin-aldosterone system (RAAS) inhibition therapy in ARAS. METHODS:...

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Detalles Bibliográficos
Autores principales: Zhang, Yanqin, Böckhaus, Jan, Wang, Fang, Wang, Suxia, Rubel, Diana, Gross, Oliver, Ding, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370956/
https://www.ncbi.nlm.nih.gov/pubmed/33772369
http://dx.doi.org/10.1007/s00467-021-05040-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370956/
https://www.ncbi.nlm.nih.gov/pubmed/33772369
http://dx.doi.org/10.1007/s00467-021-05040-9

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