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Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Alport Syndrome: A Primer for Clinicians

14 Oct 2021

Abstract excerpt

, that affects the glomerular basement membrane of the kidney. It is a rare disease with an underestimated prevalence. Genetic analysis of population cohorts has revealed that it is the second most common inherited kidney disease after polycystic kidney disease. Renal involvement is the main manifestation, although it may have associated extrarenal manifestations such as hearing loss or ocular problems. The...

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Share to Coagulation, Bradykinin, Polyphosphates, and Angioedema
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PMID: 34681722
DOI: 10.3390/ijms222011063

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