Fibromuscular Dysplasia (FMD) is evolving from a rare disease of renal arteries accounting for a minority of cases of secondary hypertension in young women, to a ‘systemic’ vascular disease which can also affect cervico-cephalic, coronary, and iliac arteries.
This is an RSM and Medics 4 Rare Diseases joint event where clinicians at all stages of their training, will be informed about why rare diseases are important to everyday medicine.
28 February 2019 will be the twelfth international Rare Disease Day coordinated by EURORDIS.
KCL MedGenSoc presents: A Talk on Haemophilia We are honoured to be hosting no less than two guest speakers for this event; KCH Haematology Consultant Dr Catherine Rea, who specialises in clotting disorders YouTuber Luke Pembroke, who himself suffers from Haemophilia Refreshments will be served before and after the talk. A sign up for a […]
Hear expert nephrologists from clinical and academic fields present the latest updates and developments in a variety of rare disease areas.
Leading experts will explore the pathophysiology of PKU, the impact of high phenylalanine levels on the brain of adult patients and the effect of PKU and aging.
Well-known experts in the epigenetics world such as; Professor Wolf Reik, Professor Stephan Beck, Professor Sir Adrian Bird, and Dr Nessa Carey will come together and give awe-inspiring talks across the epigenetics spectrum.
This conference will delve into some of the perceived mysteries and issues associated with ‘complex’ neurological conditions, in an attempt to make them less ‘complex’, and help you to address some of the unmet care needs of the people living complex neurological disorders.
CRDN are hosting a Rare Disease session as part of the new Cambridge Biotech Week Health Horizons Forum.Health Horizons is a high calibre, two-day conference focusing on the future of the healthcare industry. Created by the Global Innovation Forum.
The British Paediatric Surveillance Unit invites you to this year's event to enjoy afternoon tea and cakes, hear young people speak about their experience of living with rare disease and visit informational stands.
