A case report of CRB2 mutation identified in a Chinese boy with focal segmental glomerulosclerosis

RATIONALE: Focal segmental glomerulosclerosis (FSGS) is a common disease resulting in end-stage renal disease. The incidence of FSGS is increasing in Western countries. The clinical manifestations include proteinuria, hypoproteinemia, oedema, and hypertension. Single-gene heritable mutations are con...

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Detalles Bibliográficos
Autores principales: Fan, Jiaojiao, Fu, Rong, Ren, Fuxian, He, Junjie, Wang, Shujing, Gou, Mengfan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156060/
https://www.ncbi.nlm.nih.gov/pubmed/30212996
http://dx.doi.org/10.1097/MD.0000000000012362

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156060/
https://www.ncbi.nlm.nih.gov/pubmed/30212996
http://dx.doi.org/10.1097/MD.0000000000012362

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