Articles, insights, and posts about Child Development, early detection, and new methods in diagnosis and treatment.
Check out the new and improved AI capabilities designed to help you diagnose patients earlier (October 2022 updates): Instantly extract features from a dictated clinical note No time to write the clinical note? Simply say it and it will be written down. By clicking “Extract Features”, the relevant traits/features (HPO terms) will be suggested for […]
Manchester, Md. – KBG Foundation, a U.S.-based nonprofit organization working to improve the lives of people with KBG Syndrome, is again collaborating with FDNA to grow its Face2Gene platform, a valuable tool that can lead to earlier diagnosis of rare genetic disorders. The platform uses facial analysis technology to make it easier for physicians to […]
Face2Gene Patient Matching aims to use de-identified facial patterns and other clinical data in your case to find phenotypic similarities to other cases in Face2Gene. We will periodically scan all cases submitted to Patient Matching. If a potential match is found, you and the other clinician(s) who submitted the matching cases will be informed. If […]
DID YOU KNOW: By adding clinical features to your cases in Face2Gene, you increase the possible syndrome matches to 7,000+. NEW: Include features in each of your cases by automatically extracting HPO terms from clinical notes. How It Works 1) Copy your clinical notes to your case in Face2Gene CLINIC 2) Click the ‘Extract’ button to review the HPO* […]
FDNA’s Face2Gene technology is now being used by more than 70% of clinical geneticists at over 2,000 institutions in 130 countries. It was an exciting 2018 for FDNA, as we continued on our path to bring AI-based phenotyping technologies to clinicians, researchers, and labs globally. Take a look below for a recap of what the FDNA team […]
San Diego, CA – The FDNA team is excited to be back at the American Society of Human Genetics (ASHG) Annual Meeting, October 16-20 in San Diego and tell you more about how Face2Gene facilitates the sharing of phenotypic information with labs for improved NGS analysis. To learn more, attend our exhibitor education event, swing […]
ThinkGenetic recently hosted a panel discussion among researchers involved in the Genomics Collaborative, an FDNA initiative connecting researchers, clinicians, patients, laboratories, and advocacy groups to further disease discovery. Panel members presented their work with the collaborative, followed by a Q&A session moderated by Dawn Laney, all of which is available to watch at the bottom […]
A flock of researchers from around the globe shared their findings in dysmorphology and molecular genetics at this year’s ESHG as a part of FDNA’s corporate satellite talk and various scientific posters. Karin Weiss (Rambam Health Care Campus, Haifa, Israel) presented her further work on Sifrim Hitz Weiss Syndrome (SIHIWES), a recently described form […]
The European Society of Human Genetics (ESHG) 42nd Annual Meeting 2018 MiCo – Milano Congressi · Milan, Italy · June 16-19, 2018 Milan, Italy – I don’t know about you, but here at FDNA, we are extremely excited for an action-packed week full of presentations, posters, meetings, and, of course, gelato! Take a look […]