Fabry disease previously diagnosed as Henoch-Schonlein purpura

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Kim, Ji Hyeong (Department of Internal Medicine, Soonchunhyang University Bucheon Hospital) ;
Han, Dong Hoon (Department of Internal Medicine, Soonchunhyang University Bucheon Hospital) ;
Park, Moo Yong (Department of Internal Medicine, Soonchunhyang University Bucheon Hospital) ;
Choi, Soo Jeong (Department of Internal Medicine, Soonchunhyang University Bucheon Hospital) ;
Kim, Jin Kuk (Department of Internal Medicine, Soonchunhyang University Bucheon Hospital) ;
Hwang, Seung Duk (Department of Internal Medicine, Soonchunhyang University Bucheon Hospital) ;
Jin, So Young (Department of Pathology, Soonchunhyang University Hospital)

Supported by : Soonchunhyang University

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.

Dermatologic Aspects of Fabry Disease vol.4, pp.None, 2015, https://doi.org/10.1177/2326409816661353
Fabry disease and immunoglobulin A nephropathy presenting with Alport syndrome-like findings : A case report vol.98, pp.28, 2015, https://doi.org/10.1097/md.0000000000016256
The effect of enzyme replacement therapy on clinical outcomes in male patients with Fabry disease: A systematic literature review by a European panel of experts vol.19, pp.None, 2015, https://doi.org/10.1016/j.ymgmr.2019.100454