Cytoplasmic vacuolation consistent with Fabry disease (Q101065): Difference between revisions
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| description / pt-br | description / pt-br | ||
Depósitos de glicoesfingolípidos birrefringentes característicos são observados no citoplasma das células endoteliais e epiteliais devido à deficiência, de base genética, da enzima alfa-galactosidase A. Depósitos semelhantes também são observados em outras partes do rim. | |||
| description / en | description / en | ||
Characteristic birefringent glycosphingolipid deposits are seen in the cytoplasm of endothelial and epithelial cells due to genetically based deficiency of the enzyme alpha-galactosidase A. Similar deposits are also seen elsewhere in the kidney. | |||
Revision as of 17:51, 16 August 2026
Characteristic birefringent glycosphingolipid deposits are seen in the cytoplasm of endothelial and epithelial cells due to genetically based deficiency of the enzyme alpha-galactosidase A. Similar deposits are also seen elsewhere in the kidney.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1425331405 |
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| English | Cytoplasmic vacuolation consistent with Fabry disease |
Characteristic birefringent glycosphingolipid deposits are seen in the cytoplasm of endothelial and epithelial cells due to genetically based deficiency of the enzyme alpha-galactosidase A. Similar deposits are also seen elsewhere in the kidney. |
