Dr Andreas Brunklaus

Dr Andreas Brunklaus is a highly accomplished Consultant Paediatric Neurologist who specialises in the diagnosis and management of complex neurological conditions in children. With a primary focus on childhood epilepsies, particularly rare genetic epilepsy syndromes such as Dravet syndrome and SCN1A-related disorders, he is dedicated to delivering precise, compassionate care. His clinical work is centred on utilising advanced diagnostic tools and pioneering precision medicine programmes to tailor treatments to the unique genetic profile of each young patient.

Dr Brunklaus obtained his medical degree with First Class Honours from a prestigious medical school in Berlin, Germany. He subsequently undertook specialist training in paediatric neurology at leading tertiary children's hospitals in London before completing a research fellowship and earning his Doctor of Medicine (MD) degree from a prominent Scottish university. His doctoral thesis focused on genotype-phenotype relationships in childhood epilepsies, a contribution to child neurology that was recognised with the prestigious Mac Keith Prize by the British Paediatric Neurology Association.

In addition to his clinical practice, Dr Brunklaus is an active researcher and leader in the field of paediatric neurosciences. He serves as an Honorary Professor, leading international research collaborations to develop cutting-edge diagnostic tools and investigate novel disease-modifying therapies, including gene therapies and antisense oligonucleotides. He is a Fellow of the Royal College of Paediatrics and Child Health and holds key leadership roles, including leading a national paediatric epilepsy network and serving as Co-Chair of an international task force on clinical genetic testing.