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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Martínez-Figueroa Carlos, Cortés-Sarabia Karen, Catalán-Nájera Hilda Guadalupe, Martínez-Alarcón Micaela
Formato: article
Lenguaje:EN
ES
Publicado: De Gruyter 2020
Materias:
Acceso en línea:https://doaj.org/article/bf23a74304a24b82a4b824c7c583de10
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!