Early Detection and Follow-Up of Patients With Fabry's Disease

This research project will serve on the enhancement of early detection, diagnosis and follow-up of patients with Fabry Disease, through new biomarkers identification. This could have straight clinical impact on: 1. Early diagnosis, follow-up, and prediction of treatment response. 2. Suggestion about the optimal time to start treatment. 3. The data obtained will help to deepen our knowledge of the correlation among Lyso-Gb3, genotype and phenotype. 4. Better understanding of the pathophysiology of FD. To sum up, the results of the study will make a significant contribution to scientific knowledge providing new evidence with an immediate clinical application in FD patients. As well as, the project will serve as the basis for a large-scale project implementation to validate the results obtained