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Center for Nephrology and Metabolic Disorders: Alport Syndrome

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Description: Provides information on this genetic disorder including its pathogenesis, epidemiology, differential diagnosis and literature.
Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Alport syndrome is clinically characterized by a hereditary nephritis sensorineural deafness and a plethora of ocular abnormalities. The ultrastructural link between these different manifestations is a basement membrane disorder affecting highly differentiated basement membranes that are present in the glomerulum, organ of Corti and at some ocular localizations.
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Page title:Alport Syndrome
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IP-address:62.116.144.157

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Date
Changed: 2010-12-12T20:18:40+01:00
Changed: 2013-03-27T10:12:01+01:00
Changed: 2013-03-27T10:12:01+01:00