2019 International Congress » Pediatric Movement Disorders

1:45pm-3:15pm

Adaptor Protein Complex 4-associated Hereditary Spastic Paraplegia (AP-4-HSP): A Paradigm of Childhood-Onset Hereditary Spastic Paraplegia Caused By Defective Protein Trafficking

R. Behne, J. Teinert, M. Wimmer, S. Dwyer, A. Davies, J. Hirst, G. Borner, M. Robinson, L. Barrett, I. Chen, E. Buttermore, M. Sahin, D. Ebrahimi-Fakhari (Boston, MA, USA)

1:45pm-3:15pm

Assessment, identification and classification of movement disorders in 22q11.2 deletion syndrome

W. Fung, A. Cunningham, T. Massey, J. Hall, M. Owen, M. Van-Den-Bree, K. Peall (Newport, United Kingdom)

1:45pm-3:15pm

Deep brain stimulation in children: analysis of indication, outcome and complications

DR. Maiti (Cleveland, OH, USA)

1:45pm-3:15pm

Etiology and Clinical Study of Basal Ganglionic Lesions in a Sample of Egyptian Children

H. Zehry, S. Darwish, H. Gad, S. El Zayat, M. Tharwat, H. Emam (Dakahlyia, Egypt)

1:45pm-3:15pm

Impairment of Neurological Ontogenesis in Children with Austism Spectrum Disorders

V. Kozyavkin, T. Voloshyn (Truskavets, Ukraine)

1:45pm-3:15pm

Levodopa-responsive tremor in a young child as a delayed complication of osmotic demyelination from severe hypernatremia

L. Tochen, M. Cameron, C. Brady, M. Fleming (Washington, DC, USA)

1:45pm-3:15pm

Management of life threatening dyskinesias in GNAO1 related movement disorder: two new cases and review of the literature

M. Hull, M. Parnes (Houston, TX, USA)

1:45pm-3:15pm

MOVEMENT DISORDERS FEATURES ASSOCIATED WITH WEST SYNDROME

FS. Ngoungoure Halima, AM. Magnerou, CV. Hotcho Nganhou, M. Ndiaye, AG. Diop (Douala, Cameroon)

1:45pm-3:15pm

Novel compound heterozygous mutations in the TSFM gene causes childhood-onset chorea

CH. van Riesen, K. von Au, S. Biskup, A. Kühn, A. Kaindl, A. van Riesen (Berlin, Germany)

1:45pm-3:15pm

Opsoclonus-Myoclonus-Ataxia Syndrome – Ljubljana University Children’s Hospital clinical series

J. Orazem Mrak, D. Osredkar, D. Neubauer (Ljubljana, Slovenia)

1:45pm-3:15pm

Optimal treatment of geniospasm: a case report and review of the literature

M. Hull, M. Parnes (Houston, TX, USA)

1:45pm-3:15pm

Pantothenate kinase-associated neurodegeneration in Tunisian families

H. Benrhouma, I. Kraoua, H. Klaa, A. Rouissi, EM. Valente, I. Benyoussef Turki (Tunis, Tunisia)

1:45pm-3:15pm

Pediatric anti-N-methyl-D-aspartate receptor encephalitis associated with Coat’s-like retinal telangiectasia

N. Kumar, D. Radhakrishnana, R. Shree, G. Madhaw, R. Samanta, S. Kumari (Rishikesh, India)

1:45pm-3:15pm

Pre-status and status dystonicus in children and adolescents

G. Garone, F. Graziola, F. Nicita, F. Frascarelli, F. Randi, M. Zazza, L. Cantonetti, F. Vigevano, CE. Marras, A. Capuano (Rome, Italy)

1:45pm-3:15pm

Spectrum of Movement disorders in pediatric immune-mediated diseases

A. Saan, K. Linn, A. Minaye, C. Hlaing, K. Ko, H. Wintaung, N. Lin, Y. Wintaung (Yangon, Myanmar)

1:45pm-3:15pm

The Clinical, Molecular and Radiographic Spectrum of Adaptor Protein Complex 4-associated Hereditary Spastic Paraplegia (AP-4-HSP): Results from the AP-4-HSP International Registry

J. Teinert, R. Behne, M. Wimmer, A. Diplock, E. Carmody, K. Dies, D. Jensen, J. Bennett, M. Sahin, D. Ebrahimi-Fakhari (Boston, MA, USA)

1:45pm-3:15pm

TUBB4A mutation: Expansion of H-ABC phenotype with apparent iron accumulation in the basal ganglia – case report and literature review

C. Gorodetsky, I. Tein (Toronto, ON, Canada)