
Name
Role
I work within various areas of clinical genetics including, but not limited to, paediatrics and rare disease, adult cancer, and prenatal genetics.
I have a special interest in the genetics of cleft palate, hearing loss and connective tissue disorders.
I am also currently completing an MSt degree in genomic medicine at the University of Cambridge.
Previous history
I have a background in paediatrics and completed Level 1 training in the East of England deanery. I also worked as a clinical educator teaching medical undergraduates at Buckingham University.
I studied medicine at King's College London, graduating with an MBBS in 2013. Before that, I completed an MA in medical law and ethics at Queen Mary University of London in 2008, and a BSc (Hons) in biomedical science at King’s College London in 2007.
Membership and accreditations
- Member of the Royal College of Paediatrics and Child Health (MRCPCH)
- Collegiate member of the Royal College of Physicians (RCP)
- Member Cleft Clinical Excellence Network (CEN)
- Member of the British Society for Genetic Medicine (BSGM)
Personal interests
I work part-time to care for my family. I also enjoy running and supporting the charities Stickler Syndrome UK and CLAPA and am an amateur history enthusiast in my spare time.
Publications
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Novel antenatal presentation of cystic hygroma in a case of Koolen-de Vries syndrome
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Prospective clinical investigations of children with periodontal Ehlers-Danlos syndrome identify generalized lack of attached gingiva as a pathognomonic feature
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A neuromuscular disorder with homozygosity for PIEZO2 gene variants: an important differential diagnosis for kyphoscoliotic Ehlers-Danlos Syndrome
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Congenital muscular dystrophy - NHS