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The 2014 International Workshop on Alport Syndrome

2 Jul 2014

Abstract excerpt

Alport syndrome, historically referred to as hereditary glomerulonephritis with sensorineural deafness and anterior lenticonus, is a genetic disease of collagen α3α4α5(IV) resulting in renal failure. The collagen α3α4α5(IV) heterotrimer forms a network that is a major component of the kidney glomerular basement membrane (GBM) and basement membranes in the cochlea and eye. Alport syndrome, estimated to affect 1 in...

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PMID: 24988067
DOI: 10.1038/ki.2014.229

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