Dr Julian Raiman

Dr Julian Raiman is a Consultant Paediatrician specialising in inherited metabolic disorders and neurometabolic conditions in infants, children, and young people. He provides comprehensive diagnostic evaluations, clinical assessments, and ongoing medical care for young patients presenting with complex developmental delays, rare genetic metabolic conditions, and neurogenetic disorders. His practice focuses on delivering holistic, family-centred care that addresses each child's individual medical, physiological, and developmental requirements.

Dr Raiman possesses expertise in diagnosing and managing rare inborn errors of metabolism, lysosomal storage diseases, organic acidurias, and mitochondrial disorders. Working alongside multidisciplinary healthcare teams, he coordinates advanced diagnostic testing, enzyme replacement therapies, specialised dietary interventions, and targeted medical therapies. Dr Raiman is committed to guiding families through complex diagnostic processes, offering clear communication, evidence-based treatments, and continuous monitoring to support long-term health and developmental outcomes.

Dr Raiman obtained his Bachelor of Medicine, Bachelor of Surgery (MBBS) degree and completed a Master of Science (MSc) degree. He completed his postgraduate paediatric training in the United Kingdom and Australia, alongside specialised clinical fellowship training in paediatric metabolic genetics. He is a Member of the Royal College of Paediatrics and Child Health (MRCPCH) and actively contributes to national professional bodies, serving as a clinician representative for the British Inherited Metabolic Disease Group.