Even before birth, concerned parents often fret over the possibility that their children may have underlying medical issues. Chief among these worries are rare genetic conditions that can drastically shape the course and reduce the quality of their lives. While progress is being made in genetic testing, diagnosis of many conditions occurs only after symptoms manifest, usually to the shock of the family.
A new algorithm, however, is attempting to identify specific syndromes much sooner by screening photos for characteristic facial features associated with specific genetic conditions, such as Down’s syndrome, Progeria, and Fragile X syndrome.
via Singularity Hub
