Glomerulopathy with Fibronectin Deposits 2

Common Name(s)

Glomerulopathy with Fibronectin Deposits 2

Glomerulopathy with fibronectin deposits is a genetically heterogeneous autosomal dominant disorder characterized clinically by proteinuria, microscopic hematuria, and hypertension that leads to end-stage renal failure in the second to fifth decade of life. Pathologic examination shows enlarged glomeruli with mesangial and subendothelial fibrillary deposits that show strong immunoreactivity to fibronectin ({2:Castelletti et al., 2008}). For a discussion of genetic heterogeneity of GFND, see {137950}.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Glomerulopathy with Fibronectin Deposits 2" for support, advocacy or research.

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Scientific Literature

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

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