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Article

Two unusual cases of Anderson-Fabry disease in a Japanese family.

Clinical nephrology - 1 May 2005

Chinen S, Tana T, Kohagura K, Yamazato M, Iseki K, Takishita S

Abstract excerpt

A 16-year-old Japanese girl was admitted to our hospital on February 27, 2001, for acute renal failure. She had not shown proteinuria or hematuria in any school examination through 2000. The first renal biopsy specimen showed focal segmental glomerulosclerosis and tubulointerstitial change. Electron microscopy showed numerous myeloid bodies in the glomerular epithelium suggesting the diagnosis of Anderson-Fabry...

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PMID: 15909600
DOI: 10.5414/cnp63390

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