Cargando…

Rasmussen's Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review

Rasmussen's encephalitis (RE) is a rare progressive inflammatory disease of the central nervous system. It is characterized by unilateral hemispheric atrophy, pharmacoresistant focal seizures, and progressive neurological deficit. The exact etiopathogenesis still remains unknown. Brain imaging...

Descripción completa

Detalles Bibliográficos
Autores principales:	Klaa, Hedia, Ben Younes, Thouraya, Benrhouma, Hanene, Nagi, Sonia, Rouissi, Aida, Kraoua, Ichraf, Ben Youssef-Turki, Ilhem
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2020
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333059/ https://www.ncbi.nlm.nih.gov/pubmed/32670646 http://dx.doi.org/10.1155/2020/6810237

Ejemplares similares

Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort
por: Douma, Bissene, et al.
Publicado: (2021)

Pediatric Multiple Sclerosis in Tunisia: A Retrospective Study over 11 Years
por: Ben Achour, Nedia, et al.
Publicado: (2017)

SQSTM1 mutation: Description of the first Tunisian case and literature review
por: Akkari, M., et al.
Publicado: (2020)

ABCB1 Polymorphisms and Drug-Resistant Epilepsy in a Tunisian Population
por: Chouchi, Malek, et al.
Publicado: (2019)

Mixed movement disorders revealing an atypical form of creatine deficiency syndrome
por: Nasrallah, Fahmi, et al.
Publicado: (2015)

Novel POLR1C mutation in RNA polymerase III‐related leukodystrophy with severe myoclonus and dystonia
por: Kraoua, Ichraf, et al.
Publicado: (2019)

Mirror Movements and Myelomeningocele: Report of A Single Case and Review of Literature
por: RéBAI, Ibtihel, et al.
Publicado: (2013)

Relationship between ABCB1 3435TT genotype and antiepileptic drugs resistance in Epilepsy: updated systematic review and meta-analysis
por: Chouchi, Malek, et al.
Publicado: (2017)

Atypical Rasmussen's Encephalitis
por: Alfonso, Maria A, et al.
Publicado: (2023)

Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
por: Hechmi, Meriem, et al.
Publicado: (2022)

Pediatric anti-Hu–associated encephalitis with clinical features of Rasmussen encephalitis
por: Aravamuthan, Bhooma R., et al.
Publicado: (2015)

Rasmussen encephalitis: an older adult presentation?
por: Alvim, Ricardo Pires, et al.
Publicado: (2020)

Double Pathology in Rasmussen Encephalitis
por: Fudyma, Iga A., et al.
Publicado: (2020)

Upregulation of Adenosine Kinase in Rasmussen Encephalitis
por: Luan, Guoming, et al.
Publicado: (2013)

An immunotherapy effect analysis in Rasmussen encephalitis
por: Liba, Zuzana, et al.
Publicado: (2020)

Rasmussen’s Encephalitis: A Literary Review
por: Kumar, Abhishek, et al.
Publicado: (2023)

Valproate adverse effects on creatine metabolism and transport in a patient under drug therapy
por: Nasrallah, Fahmi, et al.
Publicado: (2014)

Evidence for Resident Memory T Cells in Rasmussen Encephalitis
por: Owens, Geoffrey C., et al.
Publicado: (2016)

Rasmussen's encephalitis presenting as focal cortical dysplasia
por: O'Rourke, D.J., et al.
Publicado: (2014)

Evidence for Resident Memory T cells in Rasmussen Encephalitis
por: Khojah, Amer, et al.
Publicado: (2016)

Rasmussen’s Epileptogenic Encephalitis in a Tropical Country
por: Assogba, Komi, et al.
Publicado: (2018)

Molecular and spatial heterogeneity of microglia in Rasmussen encephalitis
por: Westfall, Jesse J., et al.
Publicado: (2022)

Conversion disorder in children and adolescents : Clinical features of pseudoneurological symptoms
por: Gadhoum, R., et al.
Publicado: (2021)

Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
por: Mkaouar, Rahma, et al.
Publicado: (2021)

Alemtuzumab and intrathecal methotrexate failed in the therapy of Rasmussen encephalitis
por: Liba, Zuzana, et al.
Publicado: (2017)

Brain-responsive neurostimulation in adult-onset rasmussen's encephalitis
por: Feyissa, Anteneh M., et al.
Publicado: (2021)

Rasmussen’s encephalitis: mechanisms update and potential therapy target
por: Tang, Chongyang, et al.
Publicado: (2020)

Rasmussen’s encephalitis with persistent epilepsy in a young man
por: Hoang, Van Trung, et al.
Publicado: (2021)

The Diagnosis and Treatment of Rasmussen’s Encephalitis: A Case Report
por: Jadhav, Swaragandha S, et al.
Publicado: (2023)

Rituximab in Rasmussen’s encephalitis: A single center experience and review of the literature
por: Jagtap, Sujit A., et al.
Publicado: (2022)

Rasmussen encephalitis: Response to early immunotherapy in a case of immune-mediated encephalitis
por: Liba, Zuzana, et al.
Publicado: (2015)

MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy
por: Pujol, Claire, et al.
Publicado: (2022)

Rasmussen's Encephalitis with Faciobrachial Dystonic Attacks and Bilateral Hemispheric Involvement
por: Chen, Jian-Hua, et al.
Publicado: (2016)

Phenotypic and functional complexity of brain-infiltrating T cells in Rasmussen encephalitis
por: Al Nimer, Faiez, et al.
Publicado: (2017)

Genetic Factors in Rasmussen’s Encephalitis Characterized by Whole-Exome Sequencing
por: Ai, Junhong, et al.
Publicado: (2021)

The correspondence between morphometric MRI and metabolic profile in Rasmussen’s encephalitis
por: Tang, Chongyang, et al.
Publicado: (2021)

Triple Pathology in Rasmussen’s Encephalitis: A New Pathological Phenotype
por: Makkar, Ayush M., et al.
Publicado: (2022)

Globally altered microstructural properties and network topology in Rasmussen’s encephalitis
por: Held, Nina R, et al.
Publicado: (2023)

Reliability of the tunisian pediatric gait, arms, legs, and spine: toward a valid screening tool for tunisian children with musculoskeletal conditions
por: Hanene, Lassoued Ferjani, et al.
Publicado: (2023)

Inflammasome induction in Rasmussen’s encephalitis: cortical and associated white matter pathogenesis
por: Ramaswamy, Vijay, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_2m7i19eeenej49p9dfhv3648t3