Brief, case-based webinar followed by a live Q&A to provide all the information necessary for health care providers to identify the clinical and biochemical clues for diagnosing rare pediatric neurotransmitter disorders that share overlapping clinical features with each other and other neurological conditions, such as cerebral palsy, which may result in delayed diagnosis.

International Pediatric Neuroradiology Teaching Network Series

19 November Congenital Myasthenia Syndrome - an update Sithara Ramdas Oxford University Hospitals NHS Foundation Trust John Radcliffe Hospital 

Diagnostic algorithm for childhood onset chorea by Juan Dario Ortigoza-Escobar

 'Treatment of spasticity in HSP and leukodystrophies'​ by Annemieke Buizer and laura Bonouvrié

Hereditary Spastic Paraplegia - clinical disease course by Rebecca Schüle Freyer

'How can we develop and implement evidence based rehabilitation in rare disorders'​ by Hortensia Gimeno

This webinar will be delivered by Annemieke Aartsma-Rus, who is a Professor of Translational Genetics, Department of Human Genetics, Leiden University Medical Center in the Netherlands.

Topic 'A challenge in neurogenetics: Huntington disease in kids' by Ferdinando Squitieri Description Joint webinar series by the European Reference Networks for Rare Neurological Diseases (ERN-RND) and Neuromuscular Diseases (ERN-EuroNMD) and the European Academy of Neurology (EAN).