Fish-Eye Disease Latest Advances

Find the Latest Research About Fish-Eye Disease

Last Updated: 06/30/2026

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Found 512 publications

Severe HDL-C Deficiency Caused by Acquired LCAT Deficiency: A Case Report with Lipidomic Profiling and Anti-LCAT Autoantibody Detection.

Severe HDL-C Deficiency Caused by Acquired LCAT Deficiency: A Case Report with Lipidomic Profiling and Anti-LCAT Autoantibody Detection.

Journal: Internal medicine (Tokyo, Japan)
Published: May 24, 2026

Case report: co-inheritance of familial lecithin-cholesterol acyltransferase deficiency and α0-Thalassemia.

Case report: co-inheritance of familial lecithin-cholesterol acyltransferase deficiency and α0-Thalassemia.

Journal: Frontiers in genetics
Published: February 08, 2026

Ten-year clinical course of familial lecithin-cholesterol acyltransferase deficiency caused by Cys74Tyr mutation leading to dialysis and multiple systemic complications: a case report.

Ten-year clinical course of familial lecithin-cholesterol acyltransferase deficiency caused by Cys74Tyr mutation leading to dialysis and multiple systemic complications: a case report.

Journal: CEN case reports
Published: December 12, 2025

Quantitative Assessment of Visual Function in Japanese Patients With Lecithin-Cholesterol Acyltransferase Gene Abnormalities: A Case-Control Study.

Quantitative Assessment of Visual Function in Japanese Patients With Lecithin-Cholesterol Acyltransferase Gene Abnormalities: A Case-Control Study.

Journal: Cureus
Published: November 25, 2025

Diffuse corneal haze: a rare presentation of fish-eye disease.

Diffuse corneal haze: a rare presentation of fish-eye disease.

Journal: Ophthalmic genetics
Published: October 28, 2025

A Novel Missense Mutation in a Compound Heterozygous Patient with Fish-Eye Disease: A Case Report.

A Novel Missense Mutation in a Compound Heterozygous Patient with Fish-Eye Disease: A Case Report.

Journal: Case reports in ophthalmology
Published: September 28, 2025

Lecithin-Cholesterol Acyltransferase Deficiency as a Rare Cause of Bilateral Corneal Opacities: A Case Report of a Novel Frameshift Mutation.

Lecithin-Cholesterol Acyltransferase Deficiency as a Rare Cause of Bilateral Corneal Opacities: A Case Report of a Novel Frameshift Mutation.

Journal: Case reports in ophthalmology
Published: September 19, 2025

A Case of Acquired LCAT Deficiency with the Discrepancy between Spontaneous Resolution of Proteinuria and Continually Low HDL Cholesterol Levels.

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

Aberrant Cholesterol Metabolism Caused by Decreased Lecithin: Cholesterol Acyltransferase Promoted Hepatocarcinogenesis.

Aberrant Cholesterol Metabolism Caused by Decreased Lecithin: Cholesterol Acyltransferase Promoted Hepatocarcinogenesis.

Journal: Journal of hepatocellular carcinoma
Published: August 24, 2025

Short-Term Treatment for Immune-Mediated Acquired Lecithin-Cholesterol Acyltransferase Deficiency Restores the High-Density Lipoprotein Function: A Case Report.

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

Loss of LCAT function aggravates metabolic-associated steatohepatitis (MASH) in golden Syrian hamster.

Loss of LCAT function aggravates metabolic-associated steatohepatitis (MASH) in golden Syrian hamster.

Journal: Clinical science (London, England : 1979)
Published: July 07, 2025

Uncommon Factors Leading to Nephrotic Syndrome.

Uncommon Factors Leading to Nephrotic Syndrome.

Journal: Biomedicines
Published: June 29, 2025
Showing 1-12 of 512

Last Updated: 06/30/2026