3D Facial Scans Could Speed Diagnoses for Children with Rare Genetic Diseases

Scientists from Alberta, California and Colorado Merge 3D Imaging and Machine Studying to Make Prototype Diagnostic Software.

Most small children with rare genetic conditions shell out decades undergoing health care assessments and waiting for a diagnosis – a prolonged, exhausting process that normally takes its toll on small children and their families. Almost 50 % of these small children under no circumstances get a definitive diagnosis.

Now an worldwide workforce led by scientists and clinicians from the University of Colorado, University of Calgary, and UC San Francisco has developed a prototype instrument centered on 3D facial imaging that could shorten

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