Cargando…

The perioperative transition of serum biomarkers of a 1.5-year-old boy with very-long-chain acyl-CoA dehydrogenase deficiency

Very long-chain acyl-coenzyme A dehydrogenase deficiency (VLCADD, OMIM 201475) is a congenital fatty acid oxidation disorder. Individuals with VLCADD should avoid catabolic states, including strenuous exercise and long-term fasting; however, such conditions are required when undergoing surgery. The...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bo, Ryosuke, Awano, Hiroyuki, Yamada, Kenji, Ooi, Mayu, Okata, Yuichi, Bitoh, Yuko, Mizobuchi, Satoshi, Iijima, Kazumoto
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8086129/ https://www.ncbi.nlm.nih.gov/pubmed/33996489 http://dx.doi.org/10.1016/j.ymgmr.2021.100760

Ejemplares similares

Cardiac Hypertrophy in Mice with Long-Chain Acyl-CoA Dehydrogenase (LCAD) or Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
por: Cox, Keith B., et al.
Publicado: (2009)

Combined isobutyryl‐CoA and multiple acyl‐CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis
por: Tummolo, Albina, et al.
Publicado: (2022)

Two siblings with very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency suffered from rhabdomyolysis after l-carnitine supplementation
por: Watanabe, Kenji, et al.
Publicado: (2018)

Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency: Family Impact and Perspectives
por: Crawford, Sarah, et al.
Publicado: (2023)

Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency
por: Scott Schwoerer, Jessica, et al.
Publicado: (2015)

H(2)O(2) release from the very long chain acyl-CoA dehydrogenase
por: Kakimoto, Pâmela A.H.B., et al.
Publicado: (2015)

Very long‐chain acyl‐CoA dehydrogenase deficiency: No developmental delay after cardiopulmonary arrest
por: Takizaki, Nao, et al.
Publicado: (2021)

Pervasive inflammatory activation in patients with deficiency in very‐long‐chain acyl‐coA dehydrogenase (VLCADD)
por: Vallejo, Abbe N, et al.
Publicado: (2021)

Low Fasting Concentrations of Glucagon in Patients with Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
por: Stenlid, Rasmus, et al.
Publicado: (2023)

Altered Energetics of Exercise Explain Risk of Rhabdomyolysis in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
por: Diekman, E. F., et al.
Publicado: (2016)

Nutritional ketosis improves exercise metabolism in patients with very long‐chain acyl‐CoA dehydrogenase deficiency
por: Bleeker, Jeannette C., et al.
Publicado: (2020)

Structural basis for substrate specificity of methylsuccinyl-CoA dehydrogenase, an unusual member of the acyl-CoA dehydrogenase family
por: Schwander, Thomas, et al.
Publicado: (2018)

Fasting induces prominent proteomic changes in liver in very long chain Acyl-CoA dehydrogenase deficient mice
por: Wang, Wei, et al.
Publicado: (2016)

Combined HIIT and Resistance Training in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: A Case Report
por: Herrera-Olivares, Alba M., et al.
Publicado: (2019)

Clinical and molecular investigation of 37 Japanese patients with multiple acyl-CoA dehydrogenase deficiency: p.Y507D in ETFDH, a common Japanese variant, causes a mortal phenotype
por: Yamada, Kenji, et al.
Publicado: (2022)

Clinical aspects of short-chain acyl-CoA dehydrogenase deficiency
por: van Maldegem, Bianca T., et al.
Publicado: (2010)

Effects of short‐chain acyl‐CoA dehydrogenase on cardiomyocyte apoptosis
por: Zeng, Zhenhua, et al.
Publicado: (2016)

Pancreatitis in multiple acyl CoA dehydrogenase deficiency: An underdiagnosed complication
por: Elkhateeb, Nour, et al.
Publicado: (2020)

Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment
por: Mason, Emily, et al.
Publicado: (2022)

Diet-Sensitive Sources of Reactive Oxygen Species in Liver Mitochondria: Role of Very Long Chain Acyl-CoA Dehydrogenases
por: Cardoso, Ariel R., et al.
Publicado: (2013)

Renal response to short- and long-term exercise in very-long-chain acyl-CoA dehydrogenase-deficient (VLCAD(−/−)) mice
por: Tucci, Sara, et al.
Publicado: (2014)

SIRT3 and SIRT5 Regulate the Enzyme Activity and Cardiolipin Binding of Very Long-Chain Acyl-CoA Dehydrogenase
por: Zhang, Yuxun, et al.
Publicado: (2015)

Metabolic Outcomes of Anaplerotic Dodecanedioic Acid Supplementation in Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficient Fibroblasts
por: Radzikh, Igor, et al.
Publicado: (2021)

Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: High Incidence of Detected Patients With Expanded Newborn Screening Program
por: Remec, Ziga I., et al.
Publicado: (2021)

Postmortem diagnosis of very long chain acyl‐CoA dehydrogenase (VLCAD) deficiency in a neonate with sudden cardiac death
por: Singh, Prapti, et al.
Publicado: (2023)

Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Gene-Targeted Mice
por: Tolwani, Ravi J, et al.
Publicado: (2005)

Diversity and dispersal of a ubiquitous protein family: acyl-CoA dehydrogenases
por: Shen, Yao-Qing, et al.
Publicado: (2009)

Medium-Chain Acyl-CoA Dehydrogenase Deficiency in an Infant with Dilated Cardiomyopathy
por: Marcì, Marcello, et al.
Publicado: (2009)

Medium chain acyl-CoA dehydrogenase deficiency in a premature infant
por: Dobrowolski, Steven F., et al.
Publicado: (2017)

Dietary restriction in the long-chain acyl-CoA dehydrogenase knockout mouse
por: Diekman, Eugène F., et al.
Publicado: (2021)

Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Cause of Hepatomegaly
por: Nana Sede Mbakop, Raissa, et al.
Publicado: (2023)

MCT oil-based diet reverses hypertrophic cardiomyopathy in a patient with very long chain acyl-coA dehydrogenase deficiency
por: Pervaiz, Muhammad Ali, et al.
Publicado: (2011)

Long-term Correction of Very Long-chain Acyl-CoA Dehydrogenase Deficiency in Mice Using AAV9 Gene Therapy
por: Keeler, Allison M, et al.
Publicado: (2012)

Very long-/ and long Chain-3-Hydroxy Acyl CoA Dehydrogenase Deficiency correlates with deregulation of the mitochondrial fusion/fission machinery
por: Hagenbuchner, Judith, et al.
Publicado: (2018)

Molecular and clinical characteristics of very long-chain acyl-CoA dehydrogenase deficiency: A single-center experience in Saudi Arabia
por: Alhashem, Amal, et al.
Publicado: (2020)

Serum C14:1/C12:1 ratio is a useful marker for differentiating affected patients with very long-chain acyl-CoA dehydrogenase deficiency from heterozygous carriers
por: Yamada, Kenji, et al.
Publicado: (2019)

Acyl-CoA thioesterase activity of peroxisomal ABC protein ABCD1 is required for the transport of very long-chain acyl-CoA into peroxisomes
por: Kawaguchi, Kosuke, et al.
Publicado: (2021)

CR reprograms acetyl‐CoA metabolism and induces long‐chain acyl‐CoA dehydrogenase and CrAT expression
por: Mezhnina, Volha, et al.
Publicado: (2020)

Hexacosenoyl-CoA is the most abundant very long-chain acyl-CoA in ATP binding cassette transporter D1-deficient cells
por: Hama, Kotaro, et al.
Publicado: (2020)

Essential oils can cause false-positive results of medium-chain acyl-CoA dehydrogenase deficiency
por: Mikami-Saito, Yasuko, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_iokacr1d1sj3gsev14jeoffs3n