Alport syndrome
Revision as of 05:34, 28 June 2016 by Ostermayer (talk | contribs) (Created page with "==Background== A syndrome that includes kidney disease, hearing loss, and eye abnormalities. The genetic disease classically also manifests with hematuria and proteinuria as...")
Background
A syndrome that includes kidney disease, hearing loss, and eye abnormalities. The genetic disease classically also manifests with hematuria and proteinuria as the disease progresses to ESRD. Most genetic in the COL4A5 gene and are inherited in an X-linked pattern.[1]
Clinical Features
Differential Diagnosis
Diagnosis
Management
Disposition
See Also
External Links
References
- ↑ Kashtan CE. Familial hematurias: what we know and what we don't. Pediatr Nephrol. 2005 Aug;20(8):1027-35.
