Important Safety Information Indication Elfabrio ® (pegunigalsidase alfa for injection) is an enzyme replacement therapy indicated for the longterm treatment of adult patients with a confirmed ...
Health Canada has approved a new drug treatment for adults living with Fabry disease, a rare genetic disorder that can affect multiple organs and impact the quality of life.
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 ...
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 progressive condition that can come with a complex range of symptoms and complications that includes neuropathic pain, skin manifestations, and gastrointestinal issues. If left ...
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 ...
Please provide your email address to receive an email when new articles are posted on . Nephrologists often see patients with common or well-known conditions, including kidney stones, diabetes, high ...
Fabry disease is a rare condition that can run in families. The symptoms can vary from person to person, including pain or tingling in the hands and feet and a type of rash. If you are suffering from ...
Drug shortage led to kidney disease and stroke reports. Oct. 28, 2011— -- Hundreds of Fabry disease patients sickened because of a U.S. shortage of a drug that keeps them alive are hopeful they ...
Background. A 29-year-old white woman with a family history of Fabry disease was referred to a nephrology clinic with hypertension and nephropathy. Her renal function was below normal (serum ...
The Mirror US on MSN
Dad diagnosed with rare disease after dismissing aches and pains as 'aging'
Robin Schultz, 35, discovered he had Fabry disease after putting his son through genetic testing when the toddler wasn't ...
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