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About Alport Syndrome A Review
This document provides a review of Alport syndrome, a hereditary disease characterized by kidney disease, hearing loss, and eye abnormalities. It discusses the genetic basis of the disease in a defect in type IV collagen, a major component of basement membranes. This causes abnormalities in the basement membranes of the kidneys, inner ear, and eyes. Common eye findings include lenticonus (bulging of the lens) and flecked retinopathy. The document emphasizes the importance of a multidisciplinary approach to treatment given the systemic nature and impacts of the disease. Early intervention is important to address developmental delays associated with dual sensory loss from vision and hearing problems.
Detailed Information
| Author: | ['RodrigoBarrera'] |
|---|---|
| Publication Year: | 2015 |
| Pages: | 12 |
| Language: | English |
| Format: | |
| Price: | FREE |
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