Diagnostic Odyssey: Brother and sister journey to find a diagnosis for Bardet Biedl Syndrome
Lauren’s birth was déjà vu for her parents. She had extra fingers, the same as her 7-year older brother Tyler…
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Articles, insights, and posts about Child Development, early detection, and new methods in diagnosis and treatment.
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Samantha Augustyn talks about how she uses Face2Gene as a team
Continue readingThe experienced Genetic Counselor based in Florida tells us how her clinic uses Face2Gene in the workflow as a collaborative…
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Where Can We Meet During 2023
Continue readingFDNA team is gearing up for conferences and meetings in 2023, and we are excited to share with you new…
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Use Face2Gene as a Team
Continue readingCollaborate on Shared Cases with your colleagues leveraging cumulative knowledge Using Face2Gene as a TEAM allows you to securely share…
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Face2Gene helps to reduce time to diagnosis of rare genetic syndromes around the world
Continue readingTwo mothers from two different countries share a similar story: a 10 year long journey to find a diagnosis for…
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Are you sequencing upfront?
Continue readingWith this new update, healthcare providers can use Face2Gene to search for genes within the phenotypic results. A form of…
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Study finds Face2Gene AI Tech can be used to help the diagnosis of KBG Syndrome, even in remote consultations
Continue readingWe spoke with Dr. Gholson Lyon about his article that shows the utility of facial analysis to diagnose 25 KBG…
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What to do and see at ASHG 2022
Continue readingThe FDNA team is excited to be at the American Society of Human Genetics (ASHG) Annual Meeting, October 25-29 in…
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A mother’s heart knows: Nicolas’ ten-year journey to a diagnosis
Continue readingFor ten years Maria Rayane knew something was not right with her son Nicolas. She was told by different specialists…
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