We see both child and adult patients for diagnosis and management of mitochondrial disease, with genetic management being a major feature of the service. We have a multi-disciplinary service, including regular cardiology review. Further details of clinic types can be found here.
Laboratory services at the Oxford Centre comprise a specialist molecular genetic service and some specialist biochemical, cellular & histological analyses. A neuroradiology review service is also provided.
These services are primarily based within the Oxford Medical Genetics Laboratories of Oxford University Hospitals NHS Foundation Trust.
We will only accept referrals via a Neurologist, Geneticist, Paediatrician, or, in the case of positive familial testing, referrals will be accepted from a GP.
Diagnostic samples will be accepted in our laboratories with the completion of the appropriate referral documentation. Further information on the range of laboratory services is available here.
For clinical correspondence:
NHS Highly Specialised Services for Rare Mitochondrial Disorders – Oxford Centre
Nuffield Dept Obstetrics and Gynaecology
Level 3, The Women's Centre
John Radcliffe Hospital
Oxford OX3 9DU
Tel: 01865 221007
For diagnostic samples:
Oxford Medical Genetics Laboratories
Oxford University Hospitals NHS Foundation Trust
The Churchill Hospital
Oxford OX3 7LE
Tel: 01865 225594 Email: firstname.lastname@example.org