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Paediatric Movement Disorders represent a complex and heterogeneous group of neurological conditions affecting the motor control and coordination of children, encompassing a spectrum of disorders that manifest in abnormal or involuntary movements. Characterized by a wide range of symptoms, these disorders can significantly impact a child's ability to perform everyday activities, hindering their motor development and overall quality of life. Conditions such as cerebral palsy, Tourette syndrome, dystonia, and ataxia are among the myriad of disorders falling under this umbrella, each with its unique clinical presentation and underlying etiology. The intricate interplay between genetic, environmental, and neurodevelopmental factors contributes to the diversity of these disorders, making diagnosis and management challenging for healthcare professionals. Early identification and intervention are crucial to optimizing outcomes, as the developing brain exhibits remarkable plasticity. The clinical evaluation involves a multidisciplinary approach, often including neurologists, Paediatricians, physical therapists, and geneticists, who collaborate to tailor treatment plans addressing the specific needs of each child. Therapeutic interventions may encompass a combination of medications, physical and occupational therapy, and, in some cases, surgical interventions. Despite the complexities, ongoing research continues to shed light on the pathophysiology of Paediatric Movement Disorders, paving the way for innovative therapeutic strategies and fostering hope for improved prognoses and enhanced quality of life for affected children and their families.
