| Literature DB >> 27998644 |
Raphael Schiffmann1, Derralynn A Hughes2, Gabor E Linthorst3, Alberto Ortiz4, Einar Svarstad5, David G Warnock6, Michael L West7, Christoph Wanner8.
Abstract
Patients with Fabry disease (FD) are at a high risk for developing chronic kidney disease and cardiovascular disease. The availability of specific but costly therapy has elevated the profile of this rare condition. This KDIGO conference addressed controversial areas in the diagnosis, screening, and management of FD, and included enzyme replacement therapy and nonspecific standard-of-care therapy for the various manifestations of FD. Despite marked advances in patient care and improved overall outlook, there is a need to better understand the pathogenesis of this glycosphingolipidosis and to determine the appropriate age to initiate therapy in all types of patients. The need to develop more effective specific therapies was also emphasized.Entities:
Keywords: Fabry disease; Fabry nephropathy; chronic kidney disease; enzyme replacement therapy; standard of care
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Year: 2016 PMID: 27998644 DOI: 10.1016/j.kint.2016.10.004
Source DB: PubMed Journal: Kidney Int ISSN: 0085-2538 Impact factor: 10.612