Acknowledgement
Supported by : Soonchunhyang University
References
- Yoshida A, Morozumi K, Takeda A, Koyama K, Oikawa T. Fabry-like laminated myelin body associated with IgA nephropathy. Nihon Jinzo Gakkai Shi 1994;36:1303-1307.
- Kawamura O, Sakuraba H, Itoh K, et al. Subclinical Fabry's disease occurring in the context of IgA nephropathy. Clin Nephrol 1997;47:71-75.
- Pisani A, Sessa A, Sabbatini M, et al. Fabry nephropathy in a female with superposed IgA glomerulonephritis. G Ital Nefrol 2005;22:385-389.
- Whybra C, Schwarting A, Kriegsmann J, et al. IgA nephropathy in two adolescent sisters heterozygous for Fabry disease. Pediatr Nephrol 2006;21:1251-1256. https://doi.org/10.1007/s00467-006-0176-5
- Shimohata H, Yoh K, Takada K, et al. Hemizygous Fabry disease associated with IgA nephropathy: a case report. J Nephrol 2009;22:682-684.
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