Articles, insights, and posts about Child Development, early detection, and new methods in diagnosis and treatment.
En conmemoración del Día Mundial de las Personas sin Diagnóstico, el 29 de abril, la RELAGH y el FDNA hicieron un seminario web sobre la aplicación de la inteligencia artificial en enfermedades no diagnosticadas. En el evento participaron: José Elias García Ortiz, doctor en genética humana de México, quien habló sobre las enfermedades no diagnosticadas […]
In 2019, Argentina witnessed the emergence of a beacon of hope for individuals grappling with complex health challenges. The Argentine Alliance of Patients (ALAPA), a non-profit organization, came into being through the vision and determination of two remarkable women: Florencia Braga and Carolina Oliveto. Their direct connection to Stargardt disease, with Carolina as a patient […]
We asked Paula Gödke, vice president of the Brazilian Rett Syndrome Association – ABRE-TE, to tell us about the odyssey to arrive to her daughter’s diagnosis: Aline has Rett Syndrome. “I wish I had been listened to earlier, that my fears and suspicions had prompted professionals to take a second look at the case and […]
The Martin Family’s worries about their daughter Evie started early but were dismissed by health professionals. It took years for these worries to be considered and to finally get to the diagnosis of Williams Syndrome. Evie’s mother says that while microarray testing has made it easier for Williams Syndrome detection, it is dependent on a […]
Face2Gene’s Pediatrician View is a tool that aids pediatricians in evaluating the potential benefits of genetic testing for their patients. Dr. Antonio Martínez Carrascal, the Head of Pediatrician Services at Hospital de Requena, Spain, has been at the forefront of incorporating this innovative tool into his practice. Through a series of enlightening videos, Dr. Carrascal […]
In São Paulo, Brazil, we had the opportunity to get a few moments of Dr. Thais Arbocese Zanolla’s busy schedule to discuss how she uses Face2Gene in her genetics practice, where the app helps her and where it does not. As she explained it to us, Face2Gene helps her save valuable time during consultation and […]
Face2Gene is a suit of technologies that aims to help clinicians to fasten the time of diagnosis of rare and ultra-rare genetic conditions. You might know the best-of-its-class Next-Generation Phenotyping ai facial recognition use of this app, but there are more tools at your disposal that facilitate comprehensive and precise genetic evaluations. Check out all […]
Face2Gene es una plataforma digital con varias tecnologías que tiene como objetivo ayudar a los médicos a acortar el tiempo de diagnóstico de enfermedades genéticas raras. Es posible que ya esté familiarizado con el uso del reconocimiento facial de fenotipado de última generación (NGP) de esta aplicación, pero tal vez hay más herramientas a su […]
Face2Gene é um conjunto de tecnologias que visa ajudar os médicos a acelerar o tempo de diagnóstico de condições genéticas raras e ultrarraras. Você pode já conhecer o uso do reconhecimento facial de fenotipagem de última geração deste aplicativo, mas há mais ferramentas à sua disposição que facilitam avaliações genéticas abrangentes e precisas. Confira os […]