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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...

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Detalles Bibliográficos
Autores principales: Martínez-Figueroa, Carlos, Cortés-Sarabia, Karen, Catalán-Nájera, Hilda Guadalupe, Martínez-Alarcón, Micaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2020
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