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.
Artículo
en Inglés
| WPRIM
| ID: wpr-687951
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.
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WPRIM (Pacífico Occidental)
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Revista:
Chinese Medical Sciences Journal
Año:
2018
Tipo del documento:
Artículo
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