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Mulberry bodies in the urine sediment of a patient with chronic kidney disease
OBJECTIVES: 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 accumu...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
De Gruyter
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197970/ https://www.ncbi.nlm.nih.gov/pubmed/37361502 http://dx.doi.org/10.1515/almed-2020-0028 |