Cargando…
Genetic mutational testing of Chinese children with familial hematuria with biopsy-proven FSGS
Focal segmental glomerulosclerosis (FSGS) is a pathological lesion rather than a disease, with a diverse etiology. FSGS may result from genetic and non-genetic factors. FSGS is considered a podocyte disease due to the fact that in the majority of patients with proven-FSGS, the lesion results from de...
Autores principales: | Li, Yongzhen, Wang, Ying, He, Qingnan, Dang, Xiqiang, Cao, Yan, Wu, Xiaochuan, Mo, Shuanghong, He, Xiaoxie, Yi, Zhuwen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780091/ https://www.ncbi.nlm.nih.gov/pubmed/29138824 http://dx.doi.org/10.3892/mmr.2017.8023 |
Ejemplares similares
-
A novel likely pathogenic variant in the UMOD gene in a family with autosomal dominant tubulointerstitial kidney disease: a case report
por: Wang, Ying, et al.
Publicado: (2020) -
Clinical features and familial mutations in the coexistence of Wilson's disease and Alport syndrome: A case report
por: Wang, Ying, et al.
Publicado: (2023) -
Real-word adrenocorticotropic hormone treatment for childhood-onset nephrotic syndrome
por: Wang, Ying, et al.
Publicado: (2023) -
Lupus erythematosus panniculitis in a 10-year-old female child with severe systemic lupus erythematosus: A case report
por: Zhang, Ruolin, et al.
Publicado: (2018) -
Podocytic infolding in Schimke immuno-osseous dysplasia with novel SMARCAL1 mutations: a case report
por: Xiong, Shiqiu, et al.
Publicado: (2020)