Open AccessProteinuria in frasier syndrome
Author(s) -
Amira Peco-Antić,
Fatih Özaltın,
Vojislav Parezanović,
Gordana Miloševski-Lomić,
Verica Zdravković
Publication year - 2013
Publication title -
srpski arhiv za celokupno lekarstvo
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.135
H-Index - 17
eISSN - 2406-0895
pISSN - 0370-8179
DOI - 10.2298/sarh1310685p
Subject(s) - medicine , proteinuria , glomerulopathy , nephrotoxicity , malignancy , urology , bioinformatics , kidney , biology
Frasier syndrome (FS) is a genetic form of glomerulopathy, which results from mutations in the Wilms'tumour suppressor gene (WT1). Proteinuria in FS has been traditionally considered unresponsive to any medication and FS inevitably progresses to end stage renal failure.