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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Lecithin Acyltransferase Deficiency - »õâ 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.
    Synonyms : Deficiency, Lecithin Acyltransferase, Dyslipoproteinemic Corneal Dystrophy, Fish-Eye Disease, LCAT Deficiency, Lecithin:Cholesterol Acyltransferase Deficiency, alpha-LCAT Deficiency, alpha-Lecithin-Cholesterol Acyltransferase Deficiency, Fish Eye Disease
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 1
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