Fabry disease in the haemodialysis population: outcome of a UK screening study (SoFAH)

Fabry disease in the haemodialysis population: outcome of a UK screening study (SoFAH)

Abstract Background and hypothesis Fabry disease (FD) is an X-linked inherited disorder with an estimated prevalence among the end-stage kidney disease (ESKD) population of 0.3% in men and 0.1% in women [1]. Due to its non-specific manifestations, FD (especially the later-onset variant) is often und...

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Bibliographic Details
Main Authors: K.P. Ng, M. Sandhu, D. Banerjee, J.O. Burton, L. Crowley, T. Doulton, M.A. Hameed, R. Hamer, M. Menon, J. Nicholas, S.B. Ramakrishna, K. Shivakumar, T. Geberhiwot, I. Dasgupta
Format: Article
Language:English
Published: BMC 2025-05-01
Series:BMC Nephrology
Subjects:
Alpha-galactosidase A
Fabry disease
GLA variant
Hemodialysis
Lyso-Gb3
Online Access:https://doi.org/10.1186/s12882-025-04127-x
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