Effectiveness of immunosuppressive therapy for nephrotic syndrome in a patient with late-onset Fabry disease: a case report and literature review

BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations of the GLA gene, followed by deficiency in α-galactosidase A (α-gal) activity. Nephrotic syndrome, as the renal phenotype of FD, is unusual. Here, we report the rare case of a patient with FD with nephrotic...

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Detalles Bibliográficos
Autores principales: Fujisawa, Hironobu, Nakayama, Yosuke, Nakao, Shoichiro, Yamamoto, Ryo, Kurokawa, Yuka, Nakamura, Nao, Nagata, Akiko, Tsukimura, Takahiro, Togawa, Tadayasu, Sakuraba, Hitoshi, Fukami, Kei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918640/
https://www.ncbi.nlm.nih.gov/pubmed/31847900
http://dx.doi.org/10.1186/s12882-019-1657-7

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