Press releases

How Artificial Intelligence Detects Rare Diseases

Every year, around half a million children worldwide are born with a rare hereditary disease. Obtaining a definitive diagnosis can be difficult and time consuming. In a study of 679 patients with 105 different rare diseases, scientists from the University of Bonn and the Charité - Universitätsmedizin Berlin have shown that artificial intelligence can be used to diagnose rare diseases more efficiently and reliably. A neural network automatically combines portrait photos with genetic and patient data. The results are now presented in the journal "Genetics in Medicine".

Identifying Facial Phenotypes of Genetic Disorders Using Deep Learning

 

Pilot study suggests existence of genetic defects caused by X-radiation