Global Heart Failure Decompensation Revealing Fabry Disease: A Case Report
Siyam Hamady, OBEIDAT Saleh, ALFAKIHI Ismail, BOUCETTA Abdullah, Drighil A., Haboub M. & Bouziane M · Asian Journal of Cardiology Research · 2025
Background: Fabry disease is a rare X-linked lysosomal storage disorder caused by mutations in the GLA gene, resulting in deficient activity of α-galactosidase A and subsequent accumulation of globotriaosylceramide (Gb3) in multiple organs. Cardiac involvement may mimic hypertrop...
Open access
Research Article
10.9734/ajcr/2025/v8i1326