Fibronectin Glomerulopathy Caused by the Y973C Mutation in Fibronectin: A Case Report and Literature Review / 中国医学科学杂志(英文版)
Chinese Medical Sciences Journal
; (4): 60-63, 2018.
Article
in English
| WPRIM (Western Pacific)
| ID: wpr-687951
Responsible library:
WPRO
ABSTRACT
Fibronectin glomerulopathy is a rare autosomal dominant inherited glomerular disease associated with massive deposition of fibronectin. We recently diagnosed fibronectin glomerulopathy in a 29-year-old woman presenting nephrotic syndrome. Genetic analysis of fibronectin 1 gene showed heterozygosity for the Y973C mutation. However, this mutation was not found in her parents. She had stable renal function but persistent nephrotic proteinuria after one-year follow-up.
Full text:
Available
Database:
WPRIM (Western Pacific)
Language:
English
Journal:
Chinese Medical Sciences Journal
Year:
2018
Document type:
Article