A Renal Variant of Fabry Disease Diagnosed by the Presence of Urinary Mulberry Cells
Author:
Affiliation:
1. Department of Nephrology, Tokyo Medical University Ibaraki Medical Center, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/55/23/55_55.7367/_pdf
Reference16 articles.
1. 1. Desnick RJ, Banikazemi M, Wasserstein M. Enzyme replacement therapy for Fabry disease, an inherited nephropathy. Clin Nephrol 57: 1-8, 2002.
2. 2. Nakao S, Kodama C, Takenaka T, et al. Fabry disease: detection of undiagnosed hemodialysis patients and identification of a "renal variant" phenotype. Kidney Int 64: 801-807, 2003.
3. 3. Dincy PC, Karthik RK, Korula A, John D. Fabry's disease. J Assoc Physicians India 56: 242, 2008.
4. 4. Sawada K, Mizoguchi K, Hishida A, et al. Point mutation in the alpha-galactosidase A gene of atypical Fabry disease with only nephropathy. Clin Nephrol 45: 289-294, 1996.
5. 5. Meroni M, Spisni C, Tazzari S, et al. Isolated glomerular proteinuria as the only clinical manifestation of Fabry's disease in an adult male. Nephrol Dial Transplant 12: 221-223, 1997.
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