Cargando…
A Novel Mutation of UMOD in a Chinese Family with IgA Nephropathy: A Case Report
IgA nephropathy (IgAN) is the most prevalent primary glomerulonephritis worldwide, with varying clinical presentations. The hereditary susceptibility to IgAN is rather complex. In this report, a Chinese case of IgAN was recruited. Renal biopsy showed the tubular atrophy and dilatation, but the glome...
Autores principales: | Li, Furong, Zou, Huan, Liu, Li, Xiao, Tangli, Zhang, Bo, Zhang, Jun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601884/ https://www.ncbi.nlm.nih.gov/pubmed/37900933 http://dx.doi.org/10.1159/000531891 |
Ejemplares similares
-
UMOD polymorphism rs12917707 is not associated with severe or stable IgA nephropathy in a large Caucasian cohort
por: Dinic, Miriana, et al.
Publicado: (2014) -
IgA Nephropathy: A Chinese Perspective
por: Zhang, Zhao, et al.
Publicado: (2021) -
Type IV Collagen Mutations in Familial IgA Nephropathy
por: Li, Yifu, et al.
Publicado: (2020) -
A novel heterozygous missense mutation in the UMOD gene responsible for Familial Juvenile Hyperuricemic Nephropathy
por: Calado, Joaquim, et al.
Publicado: (2005) -
A Novel UMOD Mutation (c.187T>C) in a Korean Family with Juvenile Hyperuricemic Nephropathy
por: Lee, Mi-Na, et al.
Publicado: (2013)