Abstract:
Alport syndrome is a rare but significant genetic disorder that affects
multiple systems of the body, including the kidneys, hearing, and vision. It is one of the
leading causes of inherited kidney failure, which progresses with age. Despite
advancements in diagnostics and treatment, issues of early detection and appropriate
therapy remain relevant in nephrology, ophthalmology, and otolaryngology. Effective
treatment and early diagnosis are crucial for slowing disease progression and improving
the quality of life of patients.
