Isolated Proteinuria Caused by CUBN Gene Mutations: A Case Report and Review of the Literature

Mutations in the cubilin (CUBN) gene commonly cause Imerslund-Gräsbeck syndrome, while isolated proteinuria as a result of CUBN variations is rarely reported. The clinical manifestation is mainly chronic isolated proteinuria in the non-nephrotic range. However, findings to date suggest that isolated...

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Detalles Bibliográficos
Autores principales: Ran, Jingyang, Chen, Qingsong, Hu, Yudong, Yang, Pengfei, Yu, Guiquan, Liao, Xiaohui, Lei, Jianrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Case and Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293958/
https://www.ncbi.nlm.nih.gov/pubmed/37384121
http://dx.doi.org/10.1159/000530466

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293958/
https://www.ncbi.nlm.nih.gov/pubmed/37384121
http://dx.doi.org/10.1159/000530466

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