What is another word for Fabry Disease?
Pronunciation: [fˈabɹi dɪzˈiːz] (IPA) 
Fabry disease, also known as Anderson-Fabry disease, is a rare inherited disorder that affects how the body breaks down a fatty substance called globotriaosylceramide, leading to a buildup of this substance in various tissues throughout the body. Other synonyms used for Fabry disease include alpha-galactosidase A deficiency, angiokeratoma corporis diffusum, ceramide trihexosidosis, and GLA deficiency. Symptoms of Fabry disease can vary widely among affected individuals and may include neuropathic pain, skin lesions, gastrointestinal problems, hearing loss, and kidney dysfunction. Early diagnosis and treatment of Fabry disease are essential in minimizing the impact of symptoms and improving the quality of life for affected individuals.
