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Abstracts from the International Congress of Parkinson’s and Movement Disorders.

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2023 International Congress » Pediatric Movement Disorders

Meeting: 2023 International Congress

A clinical case of subdural hematoma caused by a tic-like head banging in a patient with neurodevelopmental disorder

R. Almeida Paroni, F. Boscaini, A. Crucianelli, L. Zoccante (Verona, Italy)

Deep Brain Stimulation Duration and Changes in Basal Ganglia Excitatory/Inhibitory Balance in Children and Young Adults with Dystonia

T. Larsh, D. Gilbert, S. Vadivelu, S. Wu (Cincinnati, USA)

Deep brain stimulation for the management of movement disorders in Rett syndrome

M. Hull, D. Curry, M. Parnes (Houston, USA)

Efficacy and safety of deutetrabenazine in children and adolescents with dyskinesia in cerebral palsy

D. Claassen, L. Dure, H. Barkay, S. Barash, G. Yiu, L. Voisin, L. Marinelli, P. Moshkov, J-M. Savola, M. Chen, N. Chaijale, M. Gordon, A. Ahn (Nashville, USA)

Hyperkinetic dystonia in dyskinetic cerebral palsy responds to combined DBS stimulation in thalamus and pallidum.

A. Zakharova, J. Maclean, T. Sanger (Orange, USA)

Movement disorders (MD) after stroke in childhood

D. Munoz, M. Troncoso, F. Balut, V. Naranjo, M. Hidalgo, I. Ruiz (Santiago, Chile)

Movement disorders in children with neurometabolic and neurodegenerative disorders: A single-center prospective study

A. Saini, S. Khanna, N. Sankhyan (Chandigarh, India)

Movement disorders in children with progressive myoclonic epilepsies

M. Ben Hafsa, H. Benrhouma, M. Jamoussi, T. Ben Younes, Z. Miladi, A. Zioudi, H. Klaa, I. Kraoua, I. Ben Youssef-Turki (Tunis, Tunisia)

Pediatric Myoclonus-Dystonia misdiagnosed as CASPR2 encephalitis – a diagnostic challenge

L. Dias, R. Pissarra, J. Fonseca, C. Melo, M. Sampaio, R. Sousa (Porto, Portugal)

Pilot study incorporating outcome measures after paediatric deep brain stimulation with patient and carer expectations and satisfaction

J. Barnacoat, S. Mohammad, K. Stewart, J. Lewis, S. Coombes, M-C. Waugh, M. Farrar, K. Alba-Concepcion, B. Owler, N. Mahant, R. Dale, S. Paget (Westmead, Australia)

TELO2 defect presenting with childhood-onset complex hyperkinetic MD

M. Novelli, S. Galosi, R. Carrozzo, L. Travaglini, L. Pollini, C. Caputi, F. Pisani, V. Leuzzi (Rome, Italy)

The phenotypic landscape and genetic profile of movement disorders in a cohort of tunisian children

M. Essid, H. Benrhouma, T. Benyounes, H. Klaa, R. Maroofian, Z. Miladi, I. Kraoua, H. Houlden, I. Ben Youssef-Turki (Tunis, Tunisia)

VPS11 associated movement disorder in a pediatric case

E. Serdaroglu, A. Serdaroglu (Ankara, Turkey)

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