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The importance of assigning a diagnosis to your cases

Face2Gene is an AI-driven tool that uses a set of proprietary algorithms engineered to learn from diagnosed patient photos to suggest likely phenotypic traits and genes to assist in feature annotation...

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O Pediatrician View em português, por Dr Pablo J. Videla Vilá

O Dr. Pablo Videla fala sobre o novo Pediatrician View, uma tecnologia recentemente desenvolvida pela FDNA Inc., e disponível no Face2Gene, que permite que os médicos recebam orientação sobre o nível...

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Quer dominar o Face2Gene? Veja os tutoriais disponíveis

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...

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¿Quieres dominar el uso del Face2Gene? Ver tutoriales

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...

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All the tutorials available to help you master Face2Gene

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...

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Using Face2Gene in the clinic even when the patient does not show clear...

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...

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Clinical cases using the Pediatrician View: Dr. Martinez Carrascal shows how...

Face2Gene’s Pediatrician View is a tool that aids pediatricians to evaluate the potential benefits of genetic testing for their patients. Dr. Antonio Martínez Carrascal, the Head of Pediatrician...

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Finding Hope: Navigating the Diagnostic Odyssey of Williams Syndrome

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...

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In Search of Answers: Paula Gödke’s Journey to her Daugther’s Rett Syndrome...

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...

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Empowering Patients: The Story of ALAPA

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...

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¿Qué utilidad tiene la IA en enfermedades no diagnosticadas? un seminario...

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...

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Webinar: A Novel Syndrome Associated With Prenatal Fentanyl Exposure

Dr. Karen Gripp, Erin Wadman & Carolina Alves talk about the delineation of a new syndrome associated with prenatal fentanyl exposure based on the study’s findings as recently published in Genetics...

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Spanish Coffin Siris Syndrome Association: Fighting for Health and Recognition 

Founded in 2017, the Spanish Coffin Siris Syndrome Association is an organization dedicated to supporting families affected by this rare genetic disorder.  In an exclusive interview with Alejandra...

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Interview with Dr. Giulia Pascolini: Unravelling the Genetic Underpinnings of...

Dr Giulia Pascolini, an esteemed Italian M.D. and Ph.D., is currently responsible for the Genetic Counselling Service of the Istituto Dermopatico dell’Immacolata (IDI-IRCCS) of Rome and is contributing...

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All the tutorials available to help you master Face2Gene

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...

View Article

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