Description du projet
A complex co-morbidity of neurodevelopmental and somatic illnesses may have a common cause
Since mapping the entire human genome nearly 20 years ago, scientists have made tremendous progress in understanding the genetic basis of many diseases. However, there is never a one-to-one link between a single gene and a single illness. Several neurodevelopmental disorders often occur together and, further, are associated with other somatic illnesses. This combination significantly affects a person's length and quality of life and there are no effective treatments. The EU-funded CANDY project is following a trail of rare and common genetic variants that are shared in many neurodevelopmental disorders and the possibility that immune dysregulation and microbiome at some point plays a role. Insight could point to personalised treatment and a drastic reduction in suffering for affected patients.
- /sciences médicales et de la santé/médecine fondamentale/neurologie/épilepsie
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Régime de financementRIA - Research and Innovation action