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Hughes et al. Rare Dis Orphan Drugs J 2024;3:29  https://dx.doi.org/10.20517/rdodj.2024.30  Page 3 of 3

               As we further explore the multifaceted landscape of Fabry disease through this Special Issue, we are pleased
               to announce the upcoming release of Book 2, which will further enrich our understanding and provide a
               comprehensive view of the complexities associated with this disorder. This anticipated volume will tackle
               critical aspects crucial for both clinicians and researchers committed to improving the lives of those affected
               by Fabry disease.


               DECLARATIONS
               Authors’ contributions
               Conception, design, and writing of  the article: Hughes D, Pintos-Morell G

               Availability of data and materials
               Not applicable.

               Financial support and sponsorship
               None.


               Conflicts of interest
               Both authors declared that there are no conflicts of interest.


               Ethical approval and consent to participate
               Not applicable.


               Consent for publication
               Not applicable.


               Copyright
               © The Author(s) 2024.


               REFERENCES
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               3.       de Duve C. Tissue fraction-past and present. J Cell Biol 1971;50:20.  PubMed
               4.       Brady RO, Gal AE, Bradley RM, Martenson E, Warshaw AL, Laster L. Enzymatic defect in Fabry's disease. Ceramidetrihexosidase
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               5.       Desnick RJ, Brady R, Barranger J, et al. Fabry disease, an under-recognized multisystemic disorder: expert recommendations for
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               6.       Schiffmann R. Investigating Fabry disease - some lessons learned. Rare Dis Orphan Drugs J 2024;3:4.  DOI
               7.       Feriozzi S, Rozenfeld P. The inflammatory pathogenetic pathways of Fabry nephropathy. Rare Dis Orphan Drugs J 2024;3:11.  DOI
               8.       Aguiar P. Biomarkers in anderson-Fabry disease: what should we use in the clinical practice? Rare Dis Orphan Drugs J 2024;3:13.
                   DOI
               9.       West ML, Geldenhuys L, Bichet DG. Fabry nephropathy: a treatable cause of chronic kidney disease. Rare Dis Orphan Drugs J
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               10.      Politei JM, Solar B. Gastrointestinal involvement in Fabry disease. Rare Dis Orphan Drugs J 2024;3:10.  DOI
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