With our topic “Genetics Meets Environment” we will focus on the influence of environmental factors on inherited metabolic diseases. The environment shapes health and disease and the interplay of inborn errors of metabolism and environmental factors is more relevant than ever.
PROGRAMME L’Institut des Maladies rares aux Cliniques universitaires Saint-Luc Prof. Marie-Cécile Nassogne, Cliniques universitaires Saint-Luc Besolve RD - The Belgian solution for solving rare diseases - a pilot project Prof. Joris Vermeesch, KU Leuven Enjeux économiques de l’innovation dans les maladies rares Prof. Sandy Tubeuf, Université catholique de Louvain RaDiOrg - Point de vue et […]
Each Year, UMDF’s Mitochondrial Medicine Symposium brings together the best minds in mitochondrial medicine and the patients we serve. With over 700 attendees representing almost every state in the U.S. and more than 15 different countries, the Symposium is recognized as the world’s preeminent event for mitochondrial disease. Our 2022 Symposium takes place at the […]
3rd CNE International Cystinosis Conference We are delighted to announce that the 2022 CNE International Conference will be held in Leuven, Belgium on 7-10 July. We look forward to our friends and colleagues joining us for the scientific meeting on 7 July and the family conference from 8-10 July. Covid protocols will be carefully monitored […]
The 8th Rare Disease Summer School will focus on a wide variety of subjects in the arena of rare diseases, from disease mechanisms and animal models, to improving diagnoses, to novel therapeutics. The ethical and societal challenges associated with rare diseases will also be addressed in the program. There will be lectures by national and international rare disease […]
Dear colleagues, It is with great pleasure to invite you to the third edition of the Innovation Bootcamp in Rare Diseases (IBRD2022) congress in Brussel, which will be held on October 11th 2022.The target audience of this event includes all professionals involved in the prevention, treatment and diagnosis of rare diseases and orphan drug research […]