Diet and Physical Activity in Fabry Disease: A Narrative Review
Giovanna Muscogiuri,
Oriana De Marco,
Tonia Di Lorenzo
et al.
Abstract:Fabry disease (FD) is caused by mutations in the galactosidase alpha (GLA) gene which lead to the accumulation of globotriaosylceramide (Gb-3). Enzyme replacement therapy (ERT) and oral chaperone therapy are the current pharmacological treatments for this condition. However, in the literature, there is a growing emphasis on exploring non-pharmacological therapeutic strategies to improve the quality of life of patients with FD. In particular, the nutritional approach to FD has been marginally addressed in the s… Show more
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