Fabry Disease Treatment Market Trends and Forecast to 2026
An unusual X-linked lysosomal storage condition is known as fabry disease. In this patient suffers from lack of alpha galactosidase enzyme that leads to progressive organ dysfunction. Abnormal accumulation of a specific fatty matter is called globotriaosylceramide is the mainly responsible for the development of fabry diseases. This abnormal accumulation in multiple tissues of the body is found in skin, eyes, heart, kidney, brain, gastrointestinal system, and central nervous system.
