Fetal Fentanyl Syndrome: Unveiling a New Syndrome Linked to Fentanyl Use During Pregnancy
Dr. Karen Gripp, MD, Chief of the Division of Medical Genetics at Nemours Children’s Health in Wilmington, has been at…
January 9, 2019
The Washington Times article explores the use of AI-driven facial recognition technology in diagnosing rare genetic diseases. One such tool, Face2Gene, examines patients’ facial features to detect phenotypic patterns associated with specific disorders. This cutting-edge method aids doctors in achieving faster and more precise diagnoses, especially for conditions that are difficult to identify with conventional techniques. By handling extensive datasets, the technology significantly improves diagnostic accuracy, paving the way for enhanced patient care and outcomes.
Dr. Karen Gripp, MD, Chief of the Division of Medical Genetics at Nemours Children’s Health in Wilmington, has been at…
Dr Giulia Pascolini, an esteemed Italian M.D. and Ph.D., is currently responsible for the Genetic Counselling Service of the Istituto…
Founded in 2017, the Spanish Coffin Siris Syndrome Association is an organization dedicated to supporting families affected by this rare…