Header Logo

Lecithin Cholesterol Acyltransferase Deficiency

"Lecithin Cholesterol Acyltransferase Deficiency" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

expand / collapse MeSH information
An autosomal recessive disorder of lipoprotein metabolism caused by mutation of LECITHIN CHOLESTEROL ACYLTRANSFERASE gene. It is characterized by low HDL-cholesterol levels, and the triad of CORNEAL OPACITIES; HEMOLYTIC ANEMIA; and PROTEINURIA with renal failure.


expand / collapse publications
This graph shows the total number of publications written about "Lecithin Cholesterol Acyltransferase Deficiency" by people in this website by year, and whether "Lecithin Cholesterol Acyltransferase Deficiency" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
_