Fabry disease as a trigger of immune-mediated glomerular disease: Clinical hypotheses and literature review

Fabry disease as a trigger of immune-mediated glomerular disease: Clinical hypotheses and literature review

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Fabry disease (FD) is an X-linked genetic disorder characterized by alpha-galactosidase deficiency, leading to the accumulation of globotriaosylceramide. This accumulation causes multi-organ dysfunction, with renal involvement being particularly significant. Recently, the immunological relationship...

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Bibliographic Details
Main Authors: Javier Martínez de Victoria Carazo, Haylen Marin, Francisco Javier De la Hera Fernández, Carlos Mañero Rodríguez, César Ramírez Tortosa, José Luís Callejas Rubio
Format: Article
Language:English
Published: Elsevier 2025-05-01
Series:Nefrología (English Edition)
Subjects:
Enfermedad de Fabry
Vasculitis
Glomerulonefritis
Online Access:http://www.sciencedirect.com/science/article/pii/S2013251425000641
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