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SHR Neuro Cancer Cardio Lipid Metab Microb

Brcić, I; Brcić, L; Kuzmanić, D; Corić, M; Corić, M.
Fibronectin glomerulopathy in a 34-year-old man: a case report.
Ultrastruct Pathol. 2010; 34(4): 240-242. Doi: 10.3109/01913121003783209 (- Case Report)
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Leading authors Med Uni Graz
Brcic Iva
Co-authors Med Uni Graz
Brcic Luka
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Abstract:
Fibronectin glomerulopathy is an inherited non-immune-mediated glomerulopathy associated with the massive deposition of fibronectin. It presents with proteinuria, microscopic hematuria, and hypertension that lead to end-stage renal failure in the second to sixth decade of life. A 34-year-old male was referred with proteinuria (6 g/day), microscopic hematuria and hypertension (220/130 mmHg). Renal biopsy specimen showed massive deposits of fibronectin in the mesangium and subendothelial spaces. After 20 months of multidrug treatment his renal function is stable.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Fibronectins - metabolism
Glomerular Mesangium - metabolism Glomerular Mesangium - ultrastructure
Hematuria - drug therapy Hematuria - genetics Hematuria - pathology
Humans -
Hypertension - drug therapy Hypertension - genetics Hypertension - pathology
Kidney Diseases - drug therapy Kidney Diseases - genetics Kidney Diseases - metabolism Kidney Diseases - pathology
Kidney Glomerulus - metabolism Kidney Glomerulus - pathology
Male -
Microscopy, Electron, Transmission -
Proteinuria - drug therapy Proteinuria - genetics Proteinuria - pathology
Treatment Outcome -

Find related publications in this database (Keywords)
electron microscopy
fibronectin
glomerulopathy
immunofluorescence
proteinuria
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