A 10-year-old Boy with Microscopic Hematuria and Renal Biopsy Findings Mimicking Fabry Disease
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of the enzyme α-galactosidase A, resulting in the accumulation of glycosphingolipids within the lysosomes of various cell types. It has a wide spectrum of clinical phenotypes, and renal failure is a serious complication....
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Korean Society of Pediatric Nephrology,
2016-10-01T00:00:00Z.
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