Where Can We Meet During 2023
FDNA team is gearing up for conferences and meetings in 2023, and we are excited to share with you new Read more
FDNA Insights
Use Face2Gene as a Team
Collaborate on Shared Cases with your colleagues leveraging cumulative knowledge Using Face2Gene as a TEAM allows you to securely share Read more
Face2Gene helps to reduce time to diagnosis of rare genetic syndromes around the world
Two mothers from two different countries share a similar story: a 10 year long journey to find a diagnosis for Read more
Face2Gene now allows for Reverse Phenotyping
With this new update, healthcare providers can use Face2Gene to search for genes within the phenotypic results. A form of Read more
Study finds Face2Gene AI Tech can be used to help the diagnosis of KBG Syndrome, even in remote consultations
We spoke with Dr. Gholson Lyon about his article that shows the utility of facial analysis to diagnose 25 KBG Read more
A mother’s heart knows: Nicolas’ ten-year journey to a diagnosis
For ten years Maria Rayane knew something was not right with her son Nicolas. She was told by different specialists Read more
What’s new in Face2Gene?
Check out the new and improved AI capabilities designed to help you diagnose patients earlier (October 2022 updates): Instantly extract Read more
First Patient Diagnosed with Ultra-Rare Genetic Syndrome with the help of FDNA’s new AI Algorithm
Dr. Himanshu Goel utilized FDNA’s Artificial intelligence that instantaneously matches rare disease patients’ photos with other patients’ photos around the Read more
A conversation with a Geneticist: Dr. Tinatin Tkemaladze from Tbilisi, Georgia
Dr. Tinatin Tkemaladze is the Head of the Department of Molecular and Medical Genetics at Tbilisi State Medical University, the Read more
A Diagnostic Odyssey: It took almost 10 years for Glenn “Bug” Maughan’s family to find out he had KBG Syndrome
“When you know, when it has a name, even if it doesn’t have a cure, you can find a new Read more
Webinar: Matching ultra-rare cases in the clinic
Check out now the recording of the webinar that took place on June 3rd, 2022 about matching ultra-rare cases in Read more
KBG Foundation partnered with FDNA to help improve earlier diagnose of KBG Syndrome
Manchester, Md. – KBG Foundation, a U.S.-based nonprofit organisation working to improve the lives of people with KBG Syndrome, is Read more
ACMG Meeting 2022
The FDNA team is gearing up for ACMG 2022 and we’re excited to share with you new developments and updates Read more
Precision Medicine and the Integration of Next-Generation Phenotyping
By Dr. Karen Gripp, Chief Medical Officer at FDNA Next-generation phenotyping (NGP) is characterized by the use of computer learning Read more
2019 Highlights
2019 was a year of activism, shifts in political ideology, and tech innovation, all resulting in a pause for reflection Read more
AI-Driven Facial Analysis Equals Better Healthcare for All
The world is bearing witness to a technological revolution that fundamentally changes how we do everything from creating music, Read more
Using Face2Gene to End a 12-Year-Long Diagnostic Odyssey for Mother and Daughter
In this case, Face2Gene helped Dr. Cyndy Curry by motivating targeted genetic testing for a family that had long gone Read more
Using Face2Gene to Focus Analysis on the Relevant Gene Based on Phenotype
In this case, Face2Gene helped Dr. Lynne Bird focus analysis on a single variant in a setting where the patient Read more
Using Face2Gene to Make Sense of a Medical Mystery
In this case, Face2Gene helped Dr. Li target analysis of a gene which otherwise would not have been analyzed, ultimately Read more
Using Face2Gene to Support Molecular Diagnostics in a Telehealth Setting – Case 2
After a successful experience using Face2Gene in his telehealth clinic in Scottsbluff, Dr. Abdul-Rahman decided to start another clinic using Read more
Using Face2Gene to Support Molecular Diagnostics in a Telehealth Setting – Case 1
In this case, Face2Gene helped Dr. Omar Abdul-Rahman get patients tested in a more rapid, targeted way, many times before Read more
A Rare Disease Day Reflection
Rare diseases affect roughly 30 million Americans, yet only 5 percent of the estimated 7,000 known rare diseases have cures Read more