doctor detect rare genetic disease
Facial recognition will help doctors detect rare genetic disease
NHGRI medical geneticist Paul Kruszka explains that "Human malformation syndromes appear different in different parts of the world. Even experienced clinicians have difficulty diagnosing genetic syndromes in non-European populations." That's where facial recognition comes in. The NHGRI team studied the photographs of 101 participants with the rare disease from Africa, Asia and Latin America. They then developed a facial recognition tech that was able to correctly diagnose the condition 96.6 percent of the time during their trial runs.