Mulberry bodies in the urine sediment of a patient with chronic kidney disease
Fabry disease is a hereditary disease caused by a mutation in the α-galactosidase A (GLA) gene resulting in the accumulation of glycosphingolipids in different organs. Timely diagnosis is crucial for the early initiation of treatment to avoid organic dysfunction secondary to lipid accumulation. In v...
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| Auteurs principaux: | , , , |
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| Format: | article |
| Langue: | EN ES |
| Publié: |
De Gruyter
2020
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| Accès en ligne: | https://doaj.org/article/bf23a74304a24b82a4b824c7c583de10 |
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