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“Morgan is so expressive. She smiles and she lights up the room. She just loves watching what’s happening and singing…
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Articles, insights, and posts about Child Development, early detection, and new methods in diagnosis and treatment.
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FDNA Presents Rare Disease Technologies at the 2017 Precision Medicine Summit at Boston Children’s Hospital
Continue readingThe Division of Genetics and Genomics Department of Medicine at Boston Children’s Hospital will present its exciting new Fall Precision…
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Izzy’s Journey with 22q and CHD
Continue readingFDNA focused on congenital heart defect syndromes, aortopathies and other inherited heart conditions in July for the Year of Discovery. We are uniting…
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Spotlight on Inherited Heart Conditions for the Year of Discovery
Continue readingFDNA highlights inherited heart conditions in July for the Year of Discovery. We are uniting healthcare, advocacy and technology for rare…
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Facial Analysis Discoveries for CHARGE Syndrome in the Year of Discovery
Continue readingThe performance of FDNA’s facial analysis technology, Face2Gene, was recently put up to the challenge of recognizing facial features of…
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Tyler and Lauren’s Journeys with Bardet Biedl Syndrome
Continue readingFDNA highlights eye disorders in June for the Year of Discovery. We are uniting healthcare, advocacy, and technology for rare disease…
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Facial Analysis Discoveries for Sanfilippo Syndrome B (MPS IIIB)
Continue readingIn May, FDNA reached out to clinicians and patients globally as part of the Year of Discovery to collect and…
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Miriam’s Journey with MPS IIIB
Continue readingFDNA highlighted metabolic disorders and LSDs during May for the Year of Discovery. We are uniting healthcare, advocacy and technology…
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Age-specific Facial Analysis Discoveries for Overgrowth Syndromes in the Year of Discovery
Continue readingIn April 2017, FDNA analyzed patient data from syndromes categorized as Overgrowth Syndromes as part of the Year of Discovery,…
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