Pediatric anti-N-methyl-D-aspartate receptor encephalitis associated with Coat’s-like retinal telangiectasia
Objective: We report a case of 5-year-old Indian boy with non-paraneoplastic anti NMDAR encephalitis associated with Coat's like retinal telangiectasia. Background: Anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis…Deep brain stimulation in children: analysis of indication, outcome and complications
Objective: Deep brain stimulation for pediatric movement disorder has been contemplated much less than adult counterpart. We discuss the outcome of DBS int them children…MOVEMENT DISORDERS FEATURES ASSOCIATED WITH WEST SYNDROME
Objective: To describe the clinical, therapeutic and outcome features of movement disorders (MD) observed in children with West Syndrome (WS) at the Neurology Department of…Opsoclonus-Myoclonus-Ataxia Syndrome – Ljubljana University Children’s Hospital clinical series
Objective: Analysis of number, clinical characteristics and outcome of patients admitted to our department due to OMS in the past 25 years. Background: Opsoclonus-myoclonus-ataxia syndrome…Spectrum of Movement disorders in pediatric immune-mediated diseases
Objective: To study the spectrum of movement disorders in children with immune-mediated diseases in Yangon Children Hospital, Myanmar Background: Immune-mediated diseases represent expanding conditions of…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
Objective: 1) To develop a registry and natural history study for AP-4-HSP; 2) to define core clinical and radiographic features; 3) to explore genotype-phenotype correlations.…Levodopa-responsive tremor in a young child as a delayed complication of osmotic demyelination from severe hypernatremia
Objective: To describe a case of levodopa responsive tremor due to osmotic demyelination as a result of severe hypernatremia Background: Osmotic demyelination is a known…Novel compound heterozygous mutations in the TSFM gene causes childhood-onset chorea
Objective: To report the case of a young boy suffering from a severe hyperkinetic movement disorder caused by mutations in the recently described TSFM gene.…Impairment of Neurological Ontogenesis in Children with Austism Spectrum Disorders
Objective: To assess level of involvement of neurological impairment in children with Autism Spectrum Disorders (ASD). Background: Autism Spectrum Disorders are not singly related to…Etiology and Clinical Study of Basal Ganglionic Lesions in a Sample of Egyptian Children
Objective: to determine the etiology of basal ganglionic disorders in a sample of Egyptian children Background: In childhood, the metabolic activity of the basal ganglia…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.