Anderson–Fabry Disease: Focus on Ophthalmological Implications

Fabry disease (FD) is a rare X-linked lysosomal storage disorder with a broad spectrum of clinical manifestations, including severe complications, such as end-stage renal disease, hypertrophic cardiomyopathy, and cerebrovascular disease. Enzyme replacement therapy (ERT), when initiated early, has be...

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Bibliographic Details

Published in:	Life
Main Authors:	Francesca Giovannetti, Mattia D’Andrea, Federico Bracci, Andrea Frustaci, Cristina Chimenti, Pietro Mangiantini, Alessandro Lambiase, Marco Marenco
Format:	Article
Language:	English
Published:	MDPI AG 2024-11-01
Subjects:	Fabry disease lysosomal storage disorder cornea verticillata enzyme replacement therapy vessel tortuosity retinal vessel density
Online Access:	https://www.mdpi.com/2075-1729/14/12/1531