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...
Saved in:
| Main Authors: | , , , |
|---|---|
| Format: | article |
| Language: | EN ES |
| Published: |
De Gruyter
2020
|
| Subjects: | |
| Online Access: | https://doaj.org/article/bf23a74304a24b82a4b824c7c583de10 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|