Gaucher's disease is a rare hereditary illness that impairs the body's ability to break down a type of fat molecule known as glucocerebroside. This disorder is caused by mutations in the GBA gene ...

Infants with Type 2 Gaucher disease may experience symptoms such as poor muscle tone, seizures, and developmental delays, often leading to death at a young age. “Diagnosing Gaucher disease ...

Genzyme anticipates supply constraints of Cerezyme (imiglucerase), a treatment for Gaucher disease, and Fabrazyme (agalsidase beta), used to treat Fabry disease, while the facility shuts down for ...

Gaucher disease is a genetic disorder when the body is unable to break down certain fats, leading to fat accumulation in the cells. In an interview with HT Lifestyle, Dr Ankush Golhar, liver ...