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Last Updated: 10/31/2025
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Found 503 publications
A Case of Acquired LCAT Deficiency with the Discrepancy between Spontaneous Resolution of Proteinuria and Continually Low HDL Cholesterol Levels.
Journal: Journal of atherosclerosis and thrombosis
Published: September 10, 2025
Short-Term Treatment for Immune-Mediated Acquired Lecithin-Cholesterol Acyltransferase Deficiency Restores the High-Density Lipoprotein Function: A Case Report.
Journal: Journal of atherosclerosis and thrombosis
Published: August 24, 2025
IgG3κ Monoclonal Membranous Nephropathy Associated With Acquired Lecithin Cholesterol Acyltransferase Deficiency.
Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation
Published: March 30, 2025
Fish-eye disease. Altered HDL cholesterol metabolism and corneal involvement: A case report.
Journal: Endocrinologia, diabetes y nutricion
Published: March 24, 2025
A Rare Case of Autoimmune-Mediated Lecithin:Cholesterol Acyltransferase Insufficiency Manifesting as the Acute Onset of Extremely Hypo-High-Density Lipoprotein-Cholesterolemia and Spontaneous Improvement: A Case Report with a Review of the Literature.
Journal: Journal of atherosclerosis and thrombosis
Published: December 11, 2024
Novel pathogenic variant in the LCAT gene in a compound heterozygous patient with fish-eye disease and a mild phenotype.
Journal: Journal of clinical lipidology
Published: June 18, 2024
Rescue of Familial Lecithin:Cholesterol Acyltranferase Deficiency Mutations with an Allosteric Activator.
Journal: Molecular pharmacology
Published: April 13, 2024
Longitudinal analysis of clinical and laboratory biomarkers in a patient with familial lecithin: cholesterol acyltransferase deficiency (FLD) and accelerated eGFR decline: A case study.
Journal: Journal of clinical lipidology
Published: November 08, 2023
A Novel Symptomatic Lecithin-Cholesterol Acyltransferase Gene Mutation With Corneal Amyloidosis.
Journal: Cornea
Published: October 18, 2023
Familial LCAT Deficiency and Low HDL-C Levels: In silico Characterization of Two Rare LCAT Missense Mutations.
Journal: The application of clinical genetics
Published: September 01, 2023
Last Updated: 10/31/2025