Fabry's disease is an inherited condition that develops ... and swelling in their abdomen, face, hands, and feet could occur. To reduce protein levels in the urine, patients may need to use ...

2 Walton Centre for Neurology and Neurosurgery, Liverpool L9 7LJ, UK Correspondence to: Dr J P Leach, Department of Neurology, Walton Centre for Neurology and ...

OBJECTIVES To determine the natural history of Anderson-Fabry disease (AFD) as a baseline for efficacy assessment of potentially therapeutic drugs. DESIGN The first large cross sectional study of a ...

Background Fabry disease is an X-linked lysosomal storage disorder resulting from deficiency of the alpha-galactosidase A enzyme leading to accumulation of globotriaosylceramide in multiple organ ...

uab.edu Background Fabry disease (FD) is a treatable multisystem disease caused by a defect in the alpha-galactosidase gene. Ocular signs of FD, including corneal verticillata, are among the earliest ...

amsterdamumc.nl Objective This study describes the influence of sex and disease phenotype on the occurrence of cardiac events in Fabry disease (FD). Methods Cardiac events from birth to last visit ...

The Ohio State University Wexner Medical Center’s Fabry Disease Clinic in Columbus, Ohio, is one of a select few locations in the region offering dedicated care to patients who have Fabry disease.

Amicus Therapeutics’ first oral drug for the rare condition Fabry disease has been approved by the FDA, giving patients an alternative to conventional injected enzyme replacement therapy.

ucl.ac.uk Objectives The prevalence of Anderson–Fabry disease (AFD) in patients presenting with unexplained left ventricular hypertrophy (LVH) is controversial. The aim of this study was to determine ...