Dr. Neeti Ghali

Dr. Neeti Ghali is an esteemed Consultant Clinical Geneticist and Lifestyle Medicine Physician who specialises in the diagnosis and management of rare inherited connective tissue disorders and hereditary aortovascular conditions. With extensive expertise in clinical genetics and genomics, Dr. Ghali provides comprehensive diagnostic assessments and personalised guidance to individuals and families affected by complex inherited disorders. Her compassionate, patient-centred approach ensures that patients receive tailored care and clear genetic counselling to help them understand and navigate their diagnostic findings.

In her clinical practice, Dr. Ghali focuses on evaluating individuals with suspected rare subtypes of Ehlers-Danlos syndrome, including vascular Ehlers-Danlos syndrome, as well as conditions such as Marfan syndrome, Loeys-Dietz syndrome, and non-syndromic aortopathies. She conducts thorough clinical evaluations and utilises advanced panel-based genetic testing to investigate young-onset arterial aneurysms, dissections, and strong family histories of cardiovascular or connective tissue diseases. Additionally, as a certified Lifestyle Medicine Physician, Dr. Ghali integrates evidence-based lifestyle guidance into long-term management, empowering patients to optimise their overall health and well-being alongside their genetic care.

Dr. Ghali earned her Bachelor of Medicine, Bachelor of Surgery (MBChB) from the University of Manchester in 2000. She subsequently completed specialist training in paediatrics, earning Membership of the Royal College of Paediatrics and Child Health (MRCPCH), and went on to obtain a Research Doctorate (MD) from the University of London. She is also certified by the British Society of Lifestyle Medicine. Dr. Ghali maintains professional affiliations with the Royal College of Paediatrics and Child Health and the British Society of Lifestyle Medicine, and serves on the Medical Advisory Board for Annabelle's Challenge.