Fish-eye disease (Q106503): Difference between revisions
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A doença do olho do peixe é uma forma de deficiência genética lecitina-colesterol aciltransferase (LCAT) caracterizada clinicamente por opacificações da córnea e bioquimicamente por colesterol HDL significativamente reduzido e deficiência parcial da enzima LCAT. | |||
| description / en | description / en | ||
Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterised clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency. | |||
Revision as of 13:29, 17 August 2026
Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterised clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1737717544 |
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| English | Fish-eye disease |
Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterised clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency. |
