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A case of unexpected diagnosis of fibronectin glomerulopathy with histological features of membranoproliferative glomerulonephritis

Abstract Fibronectin (FN) glomerulopathy (FNG), a rare autosomal hereditary renal disease, is characterized by proteinuria resulting from the massive accumulation of FN in the glomeruli. It typically affects individuals aged 10–50 years. In this report, we describe the case of a 57-year-old man who...

Ausführliche Beschreibung

Gespeichert in:
Hauptverfasser: Misa Hata, Takayasu Mori, Yurika Hirose, Yuriko Nishida, Shintaro Mandai, Fumiaki Ando, Koichiro Susa, Soichiro Iimori, Shotaro Naito, Eisei Sohara, Tatemitsu Rai, Towako Taguchi, Shohei Tomii, Kenichi Ohashi, Shinichi Uchida
Format: Artigo
Sprache:Inglês
Veröffentlicht: BMC 2024-01-01
Schriftenreihe:BMC Nephrology
Schlagworte:
Fibronectin glomerulopathy
Membranoproliferative Glomerulonephritis
Prednisolone
Nephrotic syndrome
Online-Zugang:https://doi.org/10.1186/s12882-024-03456-7
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