Dr Sergei Korenev

Dr Sergei Korenev is an experienced Consultant Paediatrician who specialises in paediatric metabolic medicine and inherited metabolic disorders. Dedicated to providing compassionate, child-centred care, he works closely with young patients and their families to diagnose, treat, and manage complex metabolic conditions. His practice focuses on offering reassurance, clear guidance, and individualised care pathways for children facing rare health challenges.

In his clinical practice, Dr Korenev possesses extensive expertise in the evaluation and management of rare inherited metabolic diseases, including lysosomal storage disorders such as Fabry disease, Gaucher disease, Pompe disease, and mucopolysaccharidosis. He is highly experienced in delivering advanced therapeutic interventions, including enzyme replacement therapy, and plays a key role in newborn screening initiatives designed to detect metabolic conditions at the earliest possible stage to optimise long-term health outcomes.

Dr Korenev completed his formal medical education, earning his Doctor of Medicine degree before undertaking postgraduate training in paediatric medicine. He holds membership of the Royal College of Paediatrics and Child Health. Throughout his career, he has maintained a strong commitment to professional development, remaining actively engaged in clinical research and therapeutic clinical trials aimed at advancing treatments for rare metabolic disorders.

Recognising the emotional and physical impact that complex conditions can have on families, Dr Korenev adopts a holistic and collaborative approach to paediatric care. He works alongside specialist nurses, dietitians, and therapists to deliver comprehensive support tailored to each child's specific medical and developmental needs. Through ongoing clinical research and dedicated practice, Dr Korenev strives to ensure the highest standards of care for his young patients.