Proteinuria in frasier syndrome

Proteinuria in frasier syndrome

Introduction. 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. Case Outli...

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Bibliographic Details
Main Authors: Peco-Antić Amira, Ozaltin Fatih, Parezanović Vojislav, Miloševski-Lomić Gordana, Zdravković Verica
Format: Article
Language:English
Published: Serbian Medical Society 2013-01-01
Series:Srpski Arhiv za Celokupno Lekarstvo
Subjects:
steroid resistant nephrotic syndrome
Wilms’ tumour suppressor gene (WT1)
angiotensin converting enzyme (ACE) inhibitor
angiotensin receptor blocker
indomethacin
Online Access:http://www.doiserbia.nb.rs/img/doi/0370-8179/2013/0370-81791310685P.pdf

Internet

http://www.doiserbia.nb.rs/img/doi/0370-8179/2013/0370-81791310685P.pdf

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