Familial lecithin-cholesterol acyltransferase deficiency (Q97092): Difference between revisions
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Revision as of 13:07, 16 August 2026
Familial LCAT (lecithin-cholesterol acyltransferase) deficiency (FLD) is a form of lecithin-cholesterol acyltransferase deficiency (LCAT) characterised clinically by corneal opacities, haemolytic anaemia, and renal failure, and biochemically by severely decreased HDL cholesterol and complete deficiency of the LCAT enzyme.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1147277534 |
||
| English | Familial lecithin-cholesterol acyltransferase deficiency |
Familial LCAT (lecithin-cholesterol acyltransferase) deficiency (FLD) is a form of lecithin-cholesterol acyltransferase deficiency (LCAT) characterised clinically by corneal opacities, haemolytic anaemia, and renal failure, and biochemically by severely decreased HDL cholesterol and complete deficiency of the LCAT enzyme. |
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CID11:ID_1147277534
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dki-india-ID_1147277534
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