Comparing 2D and 3D representations for face-based genetic syndrome diagnosis

Human genetic syndromes are often challenging to diagnose clinically. Facial phenotype is a key diagnostic indicator for hundreds of genetic syndromes and computer-assisted facial phenotyping is a promising approach to assist diagnosis. Most previous approaches to automated face-based syndrome diagn...

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Published inEuropean journal of human genetics : EJHG Vol. 31; no. 9; pp. 1010 - 1016
Main Authors Bannister, Jordan J., Wilms, Matthias, Aponte, J. David, Katz, David C., Klein, Ophir D., Bernier, Francois P., Spritz, Richard A., Hallgrímsson, Benedikt, Forkert, Nils D.
Format Journal Article
LanguageEnglish
Published England Nature Publishing Group 01.09.2023
Springer International Publishing
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ISSN1018-4813
1476-5438
1476-5438
DOI10.1038/s41431-023-01308-w

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Summary:Human genetic syndromes are often challenging to diagnose clinically. Facial phenotype is a key diagnostic indicator for hundreds of genetic syndromes and computer-assisted facial phenotyping is a promising approach to assist diagnosis. Most previous approaches to automated face-based syndrome diagnosis have analyzed different datasets of either 2D images or surface mesh-based 3D facial representations, making direct comparisons of performance challenging. In this work, we developed a set of subject-matched 2D and 3D facial representations, which we then analyzed with the aim of comparing the performance of 2D and 3D image-based approaches to computer-assisted syndrome diagnosis. This work represents the most comprehensive subject-matched analyses to date on this topic. In our analyses of 1907 subject faces representing 43 different genetic syndromes, 3D surface-based syndrome classification models significantly outperformed 2D image-based models trained and evaluated on the same subject faces. These results suggest that the clinical adoption of 3D facial scanning technology and continued collection of syndromic 3D facial scan data may substantially improve face-based syndrome diagnosis.
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ISSN:1018-4813
1476-5438
1476-5438
DOI:10.1038/s41431-023-01308-w