It’s now known that women, once thought to merely carry the genetic mutation that causes this disorder, can develop symptoms, although they may not be as severe as for men. Fabry disease (or ...
The rare disease can cause burning, stabbing, or shooting pain in patients. A new report details consensus findings on pain management for patients with Fabry disease. The research was published in ...
Fabry disease is a rare, inherited disease caused by the deficiency of a certain enzyme that breaks down fats in the body. Typically, a lysosomal enzyme known as alpha-galactosidase A (a-GAL A) is ...
Kidney organoids designed with the same mutation as that present in Fabry disease can help investigators better understand how the disease functions, authors suggested. A new report makes the case ...
Credit: Getty Images. Elfabrio is a hydrolytic lysosomal neutral glycosphingolipid-specific enzyme. The Food and Drug Administration (FDA) has approved Elfabrio ® (pegunigalsidase alfa-iwxj) for the ...
Fabry disease affects many parts of your body, from your heart to your digestive system. To manage it well, you need a team of doctors and other health care professionals. They'll work together to ...
DelveInsight’s Fabry Disease Market Insightsreport includes a comprehensive understanding of current treatment practices, emerging Fabry disease drugs, market share of individual therapies, and ...
If you have Fabry disease, changing what you eat may help you manage some of your symptoms. Good nutrition will also benefit your heart and kidneys. There isn't a specific Fabry disease diet. You'll ...
For Jack Johnson, getting diagnosed with Fabry disease at age 7 was more of a formality. He’d been experiencing symptoms for several years already, and had watched multiple family members struggle ...
Dublin, July 18, 2025 (GLOBE NEWSWIRE) -- The "Fabry Disease Market (By Treatment, Route of Administration, Product, End-User, Country Analysis), Key Company Profiles, Product Portfolio, Pipeline ...
Fabry disease is a rare genetic condition that belongs to a group of disorders referred to as lysosomal storage disease. This condition is also called Anderson-Fabry disease, Fabry’s disease, ...
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