Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency Latest Advances

Find the Latest Research About Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency

Last Updated: 04/28/2026

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Found 250 publications

Development and validation of a clinical severity score for long-chain fatty acid oxidation disorders using Real-World-Evidence from Canada.

Development and validation of a clinical severity score for long-chain fatty acid oxidation disorders using Real-World-Evidence from Canada.

Journal: Molecular genetics and metabolism
Published: January 08, 2026

Restoration of Interaction Between Fatty Acid Oxidation and Electron Transport Chain Proteins In Vitro by Addition of Recombinant VLCAD.

Restoration of Interaction Between Fatty Acid Oxidation and Electron Transport Chain Proteins In Vitro by Addition of Recombinant VLCAD.

Journal: Biomedicines
Published: November 28, 2025

Pregnancies in Women With Long-Chain Fatty Acid Oxidation Disorders: Results of a European and North American Survey.

Pregnancies in Women With Long-Chain Fatty Acid Oxidation Disorders: Results of a European and North American Survey.

Journal: Journal of inherited metabolic disease
Published: October 24, 2025

Direct Prediction of VLCADD Severity Using Newborn Screening Analyte Data.

Direct Prediction of VLCADD Severity Using Newborn Screening Analyte Data.

Journal: Journal of inherited metabolic disease
Published: July 15, 2025

Perioperative Management of a Patient With Very Long Chain Acyl-CoA Dehydrogenase Deficiency Undergoing Laparoscopic Sleeve Gastrectomy: First Report of Bariatric Surgery in VLCADD.

Perioperative Management of a Patient With Very Long Chain Acyl-CoA Dehydrogenase Deficiency Undergoing Laparoscopic Sleeve Gastrectomy: First Report of Bariatric Surgery in VLCADD.

Journal: Obesity surgery
Published: June 30, 2025

A Case of Adult-Onset VLCAD Deficiency.

A Case of Adult-Onset VLCAD Deficiency.

Journal: Journal of clinical neuromuscular disease
Published: June 13, 2025

Detecting mitochondrial electron transport chain enzyme defects in low-heteroplasmy single large-scale mtDNA deletion syndromes (SLSMDSs).

Detecting mitochondrial electron transport chain enzyme defects in low-heteroplasmy single large-scale mtDNA deletion syndromes (SLSMDSs).

Journal: Molecular genetics and metabolism
Published: May 16, 2025

ACADVL Deep Sequencing in a Case Study: Beyond the Common c.848T>C Pathogenic Variant.

ACADVL Deep Sequencing in a Case Study: Beyond the Common c.848T>C Pathogenic Variant.

Journal: Genes
Published: April 10, 2025

Characterization of Variants of Uncertain Significance in ACADVL Gene From a Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency Patient.

Characterization of Variants of Uncertain Significance in ACADVL Gene From a Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency Patient.

Journal: Molecular genetics & genomic medicine
Published: March 27, 2025

Myopathic Symptoms and Exercise Tolerance in Adolescent Patients With Long-Chain Fatty Acid Oxidation Disorders.

Myopathic Symptoms and Exercise Tolerance in Adolescent Patients With Long-Chain Fatty Acid Oxidation Disorders.

Journal: Journal of inherited metabolic disease
Published: March 22, 2025

Long-Chain Fatty Acid Beta-Oxidation Defects: A Case Series and Literature Review.

Long-Chain Fatty Acid Beta-Oxidation Defects: A Case Series and Literature Review.

Journal: Lipids
Published: February 27, 2025

Very long-chain acyl-CoA dehydrogenase deficiency revisited: a retrospective genotype-phenotype analysis in a Saudi tertiary center.

Very long-chain acyl-CoA dehydrogenase deficiency revisited: a retrospective genotype-phenotype analysis in a Saudi tertiary center.

Journal: Frontiers in genetics
Published: February 27, 2025
Showing 1-12 of 250

Last Updated: 04/28/2026