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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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:	chronic kidney disease fabry disease mulberry bodies Medical technology R855-855.5
Acceso en línea:	https://doaj.org/article/bf23a74304a24b82a4b824c7c583de10
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spelling	oai:doaj.org-article:bf23a74304a24b82a4b824c7c583de102021-12-05T14:10:38ZMulberry bodies in the urine sediment of a patient with chronic kidney disease2628-491X10.1515/almed-2020-0028https://doaj.org/article/bf23a74304a24b82a4b824c7c583de102020-05-01T00:00:00Zhttps://doi.org/10.1515/almed-2020-0028https://doaj.org/toc/2628-491XFabry 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 view of the above, a number of studies have been performed to assess the role of mulberry bodies as a new diagnostic tool. In this study, we report a case demonstrating the utility of this test.Martínez-Figueroa CarlosCortés-Sarabia KarenCatalán-Nájera Hilda GuadalupeMartínez-Alarcón MicaelaDe Gruyterarticlechronic kidney diseasefabry diseasemulberry bodiesMedical technologyR855-855.5ENESAdvances in Laboratory Medicine, Vol 1, Iss 3, Pp 132-8 (2020)
institution	DOAJ
collection	DOAJ
language	EN ES
topic	chronic kidney disease fabry disease mulberry bodies Medical technology R855-855.5
spellingShingle	chronic kidney disease fabry disease mulberry bodies Medical technology R855-855.5 Martínez-Figueroa Carlos Cortés-Sarabia Karen Catalán-Nájera Hilda Guadalupe Martínez-Alarcón Micaela Mulberry bodies in the urine sediment of a patient with chronic kidney disease
description	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 view of the above, a number of studies have been performed to assess the role of mulberry bodies as a new diagnostic tool. In this study, we report a case demonstrating the utility of this test.
format	article
author	Martínez-Figueroa Carlos Cortés-Sarabia Karen Catalán-Nájera Hilda Guadalupe Martínez-Alarcón Micaela
author_facet	Martínez-Figueroa Carlos Cortés-Sarabia Karen Catalán-Nájera Hilda Guadalupe Martínez-Alarcón Micaela
author_sort	Martínez-Figueroa Carlos
title	Mulberry bodies in the urine sediment of a patient with chronic kidney disease
title_short	Mulberry bodies in the urine sediment of a patient with chronic kidney disease
title_full	Mulberry bodies in the urine sediment of a patient with chronic kidney disease
title_fullStr	Mulberry bodies in the urine sediment of a patient with chronic kidney disease
title_full_unstemmed	Mulberry bodies in the urine sediment of a patient with chronic kidney disease
title_sort	mulberry bodies in the urine sediment of a patient with chronic kidney disease
publisher	De Gruyter
publishDate	2020
url	https://doaj.org/article/bf23a74304a24b82a4b824c7c583de10
work_keys_str_mv	AT martinezfigueroacarlos mulberrybodiesintheurinesedimentofapatientwithchronickidneydisease AT cortessarabiakaren mulberrybodiesintheurinesedimentofapatientwithchronickidneydisease AT catalannajerahildaguadalupe mulberrybodiesintheurinesedimentofapatientwithchronickidneydisease AT martinezalarconmicaela mulberrybodiesintheurinesedimentofapatientwithchronickidneydisease
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Mulberry bodies in the urine sediment of a patient with chronic kidney disease

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