
Alport Syndrome
Alport Syndrome is a genetic disorder that affects the kidneys, ears, and eyes. It occurs when there is a mutation in the genes responsible for producing a structural protein called collagen, which is essential for the integrity of these organs. This leads to progressive kidney damage, often resulting in kidney failure, as well as hearing loss and eye abnormalities. Symptoms can vary, and the condition is typically inherited in an X-linked pattern, affecting males more severely. Early diagnosis and management are important to slow progression and address related health issues.