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Lecithin acyltransferase deficiency: An autosomal recessively inherited disorder caused by mutation of LECITHIN CHOLESTEROL ACYLTRANSFERASE that facilitates the esterification of lipoprotein cholesterol and subsequent removal from peripheral tissues to the liver. This defect results in low HDL-cholesterol level in blood and accumulation of free cholesterol in tissue leading to a triad of CORNEAL OPACITY, hemolytic anemia (ANEMIA, HEMOLYTIC), and PROTEINURIA.
Source: MeSH 2007
These medical condition or symptom topics may be relevant to medical information for Lecithin acyltransferase deficiency:
Source - MeSH 2007
The following list attempts to classify Lecithin acyltransferase deficiency into categories where each line is subset of the next.
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