CUBN gene mutations may cause focal segmental glomerulosclerosis (FSGS) in children

BACKGROUND: Imerslund-Gräsbeck Syndrome (IGS) is mainly caused by CUBN gene biallelic mutations. Proteinuria accompanies IGS specific symptoms in about half of the patients, isolated proteinuria is rarely reported. Here we present 3 patients with isolated proteinuria and focal segmental glomeruloscl...

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Detalles Bibliográficos
Autores principales: Yang, Jing, Xu, Yongli, Deng, Linxia, Zhou, Luowen, Qiu, Liru, Zhang, Yu, Zhou, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725476/
https://www.ncbi.nlm.nih.gov/pubmed/34979989
http://dx.doi.org/10.1186/s12882-021-02654-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725476/
https://www.ncbi.nlm.nih.gov/pubmed/34979989
http://dx.doi.org/10.1186/s12882-021-02654-x

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