Cargando…
Case Report: Adolescent-Onset Isolated Nephronophthisis Caused by a Novel Homozygous Inversin Mutation
Objective: Nephronophthisis (NPHP) is a rare autosomal recessive inherited kidney disease that can cause cystic enlargement of the kidneys, and lead to end-stage renal disease (ESRD) before the age of 30 years. Herein we describe a case of adolescent-onset NPHP with a novel homozygous mutation in th...
Autores principales: | Zhong, Zhengxia, Yan, Xiaoyong, Fang, Zhengying, Dong, Yijun, Tan, Jiaxing, Xie, Jingyuan, Hu, Linhong, Zhang, Shibin, Qin, Wei |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157817/ https://www.ncbi.nlm.nih.gov/pubmed/35664325 http://dx.doi.org/10.3389/fgene.2022.847397 |
Ejemplares similares
-
Case Report: A Novel In-Frame Deletion of GLIS2 Leading to Nephronophthisis and Early Onset Kidney Failure
por: Al Alawi, Intisar, et al.
Publicado: (2021) -
Nephronophthisis
por: Salomon, Rémi, et al.
Publicado: (2008) -
Inversin/Nephrocystin-2 Is Required for Fibroblast Polarity and Directional Cell Migration
por: Veland, Iben R., et al.
Publicado: (2013) -
Phosphorylation‐dependent Akt–Inversin interaction at the basal body of primary cilia
por: Suizu, Futoshi, et al.
Publicado: (2016) -
Genetic Background and Clinicopathologic Features of Adult-onset Nephronophthisis
por: Fujimaru, Takuya, et al.
Publicado: (2021)