CHARACTERISTICS OF THE ALPORT SYNDROME THAT MANIFEST IN THE OCULAR SYSTEM

Alport syndrome (AS) is a hereditary disease that causes hearing impairment, kidney failure, and ocular abnor­malities. Because AS rare disease, it might remain undetected, meaning impacted individuals their kin have low chances of being screened receiving timely genetic counseling. Also, diagnosing requires high expertise complex technology, which are expensive for most patients. These limitations hinder them from getting the appropriate medical attention hin­ders efforts to fight it. Additionally, standard diagnos­tic method has not been established, so difficult determine prevalence accurately. This paper inves­tigates manifestations disease.