Katya has been living with kidney dysfunction for 11 years. Almost immediately after her birth, she underwent surgery to correct urological abnormalities. Doctors suspect that the cause of the disorders is Alport syndrome, a rare hereditary pathology that manifests itself in kidney failure, hearing impairment and various eye anomalies.
Katya leads an active lifestyle. Every day is timetabled. Since the age of 4, the girl has been dancing and has already had time to try herself in different directions. Last year, the schoolgirl became interested in track and field athletics. Running in the life of Katya takes a separate place. In order for the girl could continue to lead an active lifestyle, doctors need to conduct a molecular genetic study. The results will help to understand what caused the disorders and whether the girl is really threatened by Alport syndrome. An accurate diagnosis will help to prescribe timely therapy and prevent further development of the disease.
Support the girl in her fight for health, don't let the disease stop Katya.
