Cargando…

Case Report: COVID-19-Associated ROHHAD-Like Syndrome

It is known that the SARS-CoV-2 virus may cause neurologic damage. Rapid-onset obesity, hypoventilation, hypothalamus dysfunction, and autonomic dysregulation (ROHHAD) syndrome is a disease of unknown etiology with a progressive course and unclear outcomes. The etiology of ROHHAD syndrome includes g...

Descripción completa

Detalles Bibliográficos
Autores principales:	Artamonova, Irina N., Petrova, Natalia A., Lyubimova, Natalia A., Kolbina, Natalia Yu, Bryzzhin, Alexander V., Borodin, Alexander V., Levko, Tatyana A., Mamaeva, Ekaterina A., Pervunina, Tatiana M., Vasichkina, Elena S., Nikitina, Irina L., Zlotina, Anna M., Efimtsev, Alexander Yu., Kostik, Mikhail M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9009510/ https://www.ncbi.nlm.nih.gov/pubmed/35433531 http://dx.doi.org/10.3389/fped.2022.854367

Ejemplares similares

Case Report: A novel PHOX2B p.Ala248_Ala266dup variant causing congenital central hypoventilation syndrome
por: Artamonova, Irina N., et al.
Publicado: (2023)

Juvenile idiopathic arthritis with systemic onset with inflammatory bone lesions: two case reports of patients successfully treated with canakinumab and experience gained from literature
por: Alexeeva, Ekaterina I., et al.
Publicado: (2023)

Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
por: Fava, Daniela, et al.
Publicado: (2023)

ZSCAN1 Autoantibodies Are Associated with Pediatric Paraneoplastic ROHHAD
por: Mandel‐Brehm, Caleigh, et al.
Publicado: (2022)

HIDEA syndrome: A new case report highlighting similarities with ROHHAD syndrome
por: Harvengt, J., et al.
Publicado: (2023)

Ring chromosome 18 in combination with 18q12.1 (DTNA) interstitial microdeletion in a patient with multiple congenital defects
por: Zlotina, Anna, et al.
Publicado: (2016)

Whole genome sequencing in ROHHAD trios proved inconclusive: what’s beyond?
por: Grossi, A., et al.
Publicado: (2023)

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity
por: Kocaay, Pınar, et al.
Publicado: (2014)

ROHHAD syndrome and evolution of sleep disordered breathing
por: Reppucci, Diana, et al.
Publicado: (2016)

Autoimmunity Related to Adipsic Hypernatremia and ROHHAD Syndrome
por: Nakamura-Utsunomiya, Akari
Publicado: (2022)

ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison
por: Barclay, Sarah F., et al.
Publicado: (2018)

The vaccine coverage and vaccine immunity status and risk factors of non-protective levels of antibodies against vaccines in children with juvenile idiopathic arthritis: cross-sectional Russian tertiary Centre study
por: Kostik, Mikhail M., et al.
Publicado: (2021)

Necrotizing Enterocolitis: The Role of Hypoxia, Gut Microbiome, and Microbial Metabolites
por: Kaplina, Aleksandra, et al.
Publicado: (2023)

Successful treatment with tocilizumab every 4 weeks of a low disease activity group who achieve a drug-free remission in patients with systemic-onset juvenile idiopathic arthritis
por: Kostik, Mikhail M, et al.
Publicado: (2015)

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood
por: Muravyev, A., et al.
Publicado: (2022)

A Rare Cause of Sleep-Disordered Breathing: ROHHAD Syndrome
por: Özcan, Gizem, et al.
Publicado: (2020)

Thoracic Ganglioneuroma Presenting with Paraneoplastic Cerebellitis and ROHHAD-NET Syndrome
por: Tiwari, Sarbesh, et al.
Publicado: (2022)

Case Reports: Emery-Dreifuss Muscular Dystrophy Presenting as a Heart Rhythm Disorders in Children
por: Kovalchuk, Tatiana, et al.
Publicado: (2021)

Identification of the best cut-off points and clinical signs specific for early recognition of macrophage activation syndrome in active systemic juvenile idiopathic arthritis
por: Kostik, Mikhail M, et al.
Publicado: (2014)

Hepatic glycogen synthase (GYS2) deficiency: seven novel patients and seven novel variants
por: Kamenets, Elena A., et al.
Publicado: (2020)

ROHHAD syndrome without rapid-onset obesity: A diagnosis challenge
por: Desse, Blandine, et al.
Publicado: (2022)

Combined System for the Simultaneous Delivery of Levofloxacin and Rifampicin: Structural and Functional Properties and Antibacterial Activity
por: Le-Deygen, Irina M., et al.
Publicado: (2023)

Analysis and comparisons of gene expression changes in patient- derived neurons from ROHHAD, CCHS, and PWS
por: Victor, A. Kaitlyn, et al.
Publicado: (2023)

Case report: Sulfasalazine-induced hypersensitivity
por: Kuchinskaya, Ekaterina M., et al.
Publicado: (2023)

ROHHAD Syndrome, a Rare Cause of Hypothalamic Obesity: Report of Two Cases
por: Şiraz, Ülkü Gül, et al.
Publicado: (2018)

A Case Report of ROHHAD Syndrome in an 8-year-old Iranian Boy
por: Amjadipour, Abolfazl, et al.
Publicado: (2021)

Excited State Proton Transfers in Hybrid Compound Based on Indoline Spiropyran of the Coumarin Type and Azomethinocoumarin in the Presence of Metal Ions
por: Zaichenko, Natalia L., et al.
Publicado: (2021)

A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report
por: Zlotina, Anna, et al.
Publicado: (2020)

Antigen-Specific IFN-γ Responses Correlate with the Activity of M. tuberculosis Infection but Are Not Associated with the Severity of Tuberculosis Disease
por: Nikitina, Irina Yu., et al.
Publicado: (2016)

Host-Microbiome Interactions Mediated by Phenolic Metabolites in Chronically Critically Ill Patients
por: Chernevskaya, Ekaterina, et al.
Publicado: (2021)

Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours
por: Barclay, Sarah F., et al.
Publicado: (2015)

Congenital Heart Defects Are Rarely Caused by Mutations in Cardiac and Smooth Muscle Actin Genes
por: Khodyuchenko, Tatiana, et al.
Publicado: (2015)

Prolactin and growth hormone affect metaphase-II chromosomes in aging oocytes via cumulus cells using similar signaling pathways
por: Lebedeva, Irina Y., et al.
Publicado: (2015)

Case report: Molecular characterisation of adipose-tissue derived cells from a patient with ROHHAD syndrome
por: Biernacka, Kalina M., et al.
Publicado: (2023)

Recent advances in understanding genetic variants associated with growth, carcass and meat productivity traits in sheep (Ovis aries): an update
por: Zlobin, Alexander S., et al.
Publicado: (2019)

Natural history of ROHHAD syndrome: development of severe insulin resistance and fatty liver disease over time
por: Jalal Eldin, Abdel Wahab, et al.
Publicado: (2019)

Pulmonary hypertension and chronic hypoventilation in ROHHAD syndrome treated with average‐volume assured pressure support
por: Stowe, Robert C., et al.
Publicado: (2019)

Structural Features of Amyloid Fibrils Formed from the Full-Length and Truncated Forms of Beta-2-Microglobulin Probed by Fluorescent Dye Thioflavin T
por: Sulatskaya, Anna I., et al.
Publicado: (2018)

Non-Targeted Screening of Metabolites in Aqueous-Ethanol Extract from Spiraea hypericifolia (Rosaceae) Using LC-HRMS
por: Kostikova, Vera A., et al.
Publicado: (2023)

Clinical Experience of High Frequency and Low Frequency TENS in Treatment of Diabetic Neuropathic Pain in Russia
por: Al-Zamil, Mustafa, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_v09th8g3v8f64iue53p90e447h