Fabry Syndrome

Fabry syndrome

Fabry disease is a rare hereditary disease. It is characterized by the accumulation in the human body of a disease substrate consisting of glycosaminoglycans and polysaccharides. In this case, most organs and systems of the body are affected. A person may experience many symptoms including dizziness, hearing problems, vision loss, muscle weakness, kidney problems and many others. In this article, we will look at what Fabry syndrome is, how it manifests itself, and what treatments are available to patients with this disease.

1. Description of the disease

**Fabry syndrome** also known as **