Introduction: Common symptoms for children with Anderson-Fabry Disease (FD) such as acroparaesthesia and gastrointestinal manifestations can only be objectively assessed in patients using a valid ...
Fabry disease can affect various organs and causes many symptoms that also can happen with other conditions. This rare genetic disease also may trigger different symptoms and problems in different ...
A small study, based on 4 family members with Fabry disease, affirms the importance of early enzyme replacement therapy. Enzyme replacement therapy (ERT) with agalsidase-β led to long-term improvement ...
It can take a long time to get diagnosed with Fabry disease. Many people wait more than a decade after they first have symptoms to learn that they have this genetic condition. Fabry disease is often ...
Background A 64-year-old male was observed as an outpatient with atypical, non-exercise-induced chest pain and palpitations. He had arterial hypertension and marked concentric left ventricular ...
This year’s most-read articles on Fabry disease touched on advancements in therapy, health risks of the disease, and keys to improved diagnosis. The top 5 most-read Fabry disease articles of 2021 on ...
Elfabrio (R) (pegunigalsidase alfa for injection) is an enzyme replacement therapy indicated for the longterm treatment of adult patients with a confirmed diagnosis of Fabry disease (deficiency of ...
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 ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback