Fibronectin glomerulopathy (Q44653): Difference between revisions
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CID11:MF81 | |||||||||||||||
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dki-india-MF81 | |||||||||||||||
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13 August 2026
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Latest revision as of 12:13, 13 August 2026
Fibronectin glomerulopathy is a rare hereditary kidney disease in which fibronectin (FN1) deposits are seen in the mesangium and subendothelial space. The clinical picture is characterised by proteinuria, type IV renal tubular acidosis, microscopic haematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. This disease may be associated with mutations in the FN1 gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | MF81 |
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| English | Fibronectin glomerulopathy |
Fibronectin glomerulopathy is a rare hereditary kidney disease in which fibronectin (FN1) deposits are seen in the mesangium and subendothelial space. The clinical picture is characterised by proteinuria, type IV renal tubular acidosis, microscopic haematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. This disease may be associated with mutations in the FN1 gene. |
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CID11:MF81
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dki-india-MF81
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Concluído
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13 August 2026
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