Renin-angiotensin System Blockade Therapy for Early Renal Involvement in MYH9-related Disease with an E1841K Mutation

MYH9-related disease is a rare genetic disorder characterized by macrothrombocytopenia, with frequent proteinuric nephropathy, hearing loss, and cataract. Although proteinuric nephropathy usually progresses to renal failure, there is no established treatment for the nephropathy. We herein describe t...

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Detalles Bibliográficos
Autores principales: Tanaka, Mari, Miki, Sho, Saita, Hirona, Shimada, Hiroki, Nishikawa, Seira, Taniguchi, Keisuke, Hagihara, Koichiro, Iwanari, Sachio, Ikeda, Masaki, Kunishima, Shinji, Takeoka, Hiroya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859379/
https://www.ncbi.nlm.nih.gov/pubmed/31243205
http://dx.doi.org/10.2169/internalmedicine.2997-19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859379/
https://www.ncbi.nlm.nih.gov/pubmed/31243205
http://dx.doi.org/10.2169/internalmedicine.2997-19

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