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…
March 21, 2017
The article explains that FDNA has introduced an innovative app-based tool designed to aid clinicians in diagnosing and treating rare diseases. Utilizing advanced facial recognition, artificial intelligence (AI), and vast genetic data, this decision support tool provides a robust resource for healthcare professionals. The app enhances the accuracy of rare disease identification by analyzing facial features and correlating them with genetic information. This cutting-edge technology streamlines the diagnostic process, offering a significant leap forward in the early detection and management of rare conditions. By leveraging AI and big data, FDNA’s tool for clinicians is set to revolutionize rare diseases, making precise and timely diagnoses more accessible.
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…