Histopathological findings in renal biopsies in Anderson–Fabry disease. Case series
Anderson–Fabry disease is the second most common lysosomal storage disease after Gaucher disease. It is an X-linked lysosomal disorder that causes a deficiency in alpha-galactosidase, leading to the accumulation of globotriaosylceramide (Gb3) in the lysosomes of different cells, producing renal, car...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Permanyer
2018-10-01
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| Series: | Revista Médica del Hospital General de México |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S0185106316301019 |