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.
