Cargando…

Anesthetic management of a pediatric patient with Electron Transfer Flavoprotein Dehydrogenase deficiency (ETFDH) and acute appendicitis: case report and review of the literature

BACKGROUND: Mitochondria are the energy producing organelles practically in every human cell except erythrocytes. Indeed mitochondria are widespread in high energy requiring organs like brain, heart and muscles. Currently there are no clinical trials supporting with clear evidence which is the most...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lilitsis, Emmanuel, Astyrakaki, Elisavet, Blevrakis, Evaggelos, Xenaki, Sofia, Chalkiadakis, George, Chrysos, Emmanuel
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576333/ https://www.ncbi.nlm.nih.gov/pubmed/28851284 http://dx.doi.org/10.1186/s12871-017-0400-9

Ejemplares similares

Multiple magnet ingestion causing instestinal obstruction and entero-enteric fistula: Which imaging modality besides radiographs? A case report
por: Blevrakis, Evangelos, et al.
Publicado: (2018)

A case of asystole from carotid sinus hypersensitivity during patient positioning for thyroidectomy
por: Lilitsis, Emmanuel, et al.
Publicado: (2016)

Guiding Management in Severe Trauma: Reviewing Factors Predicting Outcome in Vastly Injured Patients
por: Lilitsis, Emmanuel, et al.
Publicado: (2018)

Laparoscopic repair of posttraumatic diaphragmatic rupture. Report of three cases
por: Xenaki, Sofia, et al.
Publicado: (2014)

Newly recognized extratumoral features of colorectal cancer challenge the current tumor-node-metastasis staging system
por: Athanasakis, Elias, et al.
Publicado: (2018)

A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family
por: Ou, Mingcai, et al.
Publicado: (2020)

A Rare Case of Mixed Neuroendocrine Tumor and Adenocarcinoma of the Pancreas
por: Xenaki, Sofia, et al.
Publicado: (2016)

Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency
por: Fan, Xin, et al.
Publicado: (2018)

Clinical Features of Multiple Acyl-CoA Dehydrogenase Deficiency With ETFDH Variants in the First Korean Cases
por: Kim, Yoo Jinie, et al.
Publicado: (2018)

Advanced Mesodermal (Müllerian) Adenosarcoma of the Ovary: Metastases to the Lungs, Mouth, and Brain
por: Daskalaki, A., et al.
Publicado: (2015)

Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
por: Missaglia, Sara, et al.
Publicado: (2018)

Clinical characteristics and gene mutation analysis of an adult patient with ETFDH-related multiple acyl-CoA dehydrogenase deficiency
por: Wang, Chenyi, et al.
Publicado: (2020)

Well-promising outcomes with vacuum-assisted closure in an infected wound following laparotomy: A case report
por: Daskalaki, A., et al.
Publicado: (2016)

Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report
por: Goh, Liuh Ling, et al.
Publicado: (2018)

Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD) in the ETFDH gene: A case report and a literature review
por: Ding, Meijuan, et al.
Publicado: (2020)

Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations
por: Chen, Wei, et al.
Publicado: (2019)

Early Postoperative Parathormone and Calcium as Prognostic Factors for Postoperative Hypocalcemia
por: Daskalaki, Anna, et al.
Publicado: (2022)

Correction: Daskalaki et al. Early Postoperative Parathormone and Calcium as Prognostic Factors for Postoperative Hypocalcemia. J. Clin. Med. 2022, 11, 2389
por: Daskalaki, Anna, et al.
Publicado: (2022)

The semiquinone swing in the bifurcating electron transferring flavoprotein/butyryl-CoA dehydrogenase complex from Clostridium difficile
por: Demmer, Julius K., et al.
Publicado: (2017)

A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report
por: De Pasquale, Loredana, et al.
Publicado: (2022)

Lipid storage myopathy due to late-onset multiple Acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH: A case report
por: Tian, Huihong, et al.
Publicado: (2022)

Long-Time Oxygen Localization in Electron Transfer Flavoprotein
por: Salerno, K. Michael, et al.
Publicado: (2022)

Case report: A novel c.1842_1845dup mutation of ETFDH in two Chinese siblings with multiple acyl-CoA dehydrogenase deficiency
por: Yuan, Gaopin, et al.
Publicado: (2023)

Functional characterization of electron-transferring flavoprotein and its dehydrogenase required for fungal development and plant infection by the rice blast fungus
por: Li, Ya, et al.
Publicado: (2016)

Long-term outcomes of a patient with late-onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutations in ETFDH: A case report
por: Wang, Juan, et al.
Publicado: (2018)

Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency
por: Chen, Hai-Zhu, et al.
Publicado: (2019)

A case of solitary rectal diverticulum presenting with a large retrorectal abscess
por: Gorgoraptis, Stefanos, et al.
Publicado: (2019)

Plant Flavoprotein Photoreceptors
por: Christie, John M., et al.
Publicado: (2015)

Spin Dynamics of Flavoproteins
por: Matysik, Jörg, et al.
Publicado: (2023)

Characterization of ETFDH and PHGDH Mutations in a Patient with Mild Glutaric Aciduria Type II and Serine Deficiency
por: Ali, Amanat, et al.
Publicado: (2021)

The Flavoprotein Dodecin as a Redox Probe for Electron Transfer through DNA**
por: Yu, Yaming, et al.
Publicado: (2013)

Noncovalent interactions that tune the reactivities of the flavins in bifurcating electron transferring flavoprotein
por: González-Viegas, María, et al.
Publicado: (2023)

Compound heterozygous mutations in electron transfer flavoprotein dehydrogenase identified in a young Chinese woman with late-onset glutaric aciduria type II
por: Xue, Ying, et al.
Publicado: (2017)

Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations
por: Liu, Xin-Yi, et al.
Publicado: (2016)

A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene
por: Wu, Yue, et al.
Publicado: (2020)

Factors Associated with Malnutrition and Its Impact on Postoperative Outcomes in Older Patients
por: Venianaki, Maria, et al.
Publicado: (2021)

Vertebrate Cryptochromes are Vestigial Flavoproteins
por: Kutta, Roger J., et al.
Publicado: (2017)

Two novel ETFDH mutations in a patient with lipid storage myopathy
por: Xu, Hong-Liang, et al.
Publicado: (2019)

Ethylene Glycol Monomethyl Ether–Induced Toxicity Is Mediated through the Inhibition of Flavoprotein Dehydrogenase Enzyme Family
por: Takei, Makoto, et al.
Publicado: (2010)

Internal-mesocolic hernia after laparoscopic left colectomy report of case with late manifestation
por: Daskalaki, Anna, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_t0ja7i8ics1cnpvn8r8cktu8q7