Fabry App: the value of a portable technology in recording day-to-day patient monitored information in patients with Fabry disease

Fabry disease is a rare inherited disorder resulting from deficient α-galactosidase A enzyme activity. Common disease manifestations are sweating abnormalities, neuropathic pain, gastrointestinal symptoms and ...

Source: Orphanet Journal of Rare Diseases - January 11, 2024 Category: Internal Medicine Authors: Simona D ’Amore, Mark Mckie, Andrew Fahey, David Bleloch, Giuseppina Grillo, Michael Hughes and Uma Ramaswami Tags: Research Source Type: research