Fabry Disease: Report of Two Cases with Uncommon Presentation

Fabry disease (FD) is a rare, lysosomal storage disorder characterized by multiorgan accumulation of predominantly globotriaosylceramide (GL3) and its metabolite. Resulting renal, cardiac, and cerebrovascular complications are crucial causes of morbidity and mortality in FD. Enzyme replacement thera...

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Detalles Bibliográficos
Autores principales: Prasad, Pallavi, Singh, Anshima, Yachha, Monika, Agrawal, Vinita, Pandey, Rakesh, Jain, Manoj, Bhadauria, Dharmendra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872913/
https://www.ncbi.nlm.nih.gov/pubmed/36704583
http://dx.doi.org/10.4103/ijn.ijn_263_21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872913/
https://www.ncbi.nlm.nih.gov/pubmed/36704583
http://dx.doi.org/10.4103/ijn.ijn_263_21

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