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Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorder.

Authors :
Sleyp Y
Matthews HS
Vanneste M
Vandenhove L
Delanote V
Hoskens H
Indencleef K
Teule H
Larmuseau MHD
Steyaert J
Devriendt K
Claes P
Peeters H
Source :
Clinical genetics [Clin Genet] 2024 Nov; Vol. 106 (5), pp. 603-613. Date of Electronic Publication: 2024 Jul 26.
Publication Year :
2024

Abstract

Recognizing Mendelian causes is crucial in molecular diagnostics and counseling for patients with autism spectrum disorder (ASD). We explored facial dysmorphism and facial asymmetry in relation to genetic causes in ASD patients and studied the potential of objective facial phenotyping in discriminating between Mendelian and multifactorial ASD. In a cohort of 152 ASD patients, 3D facial images were used to calculate three metrics: a computational dysmorphism score, a computational asymmetry score, and an expert dysmorphism score. High scores for each of the three metrics were associated with Mendelian causes of ASD. The computational dysmorphism score showed a significant correlation with the average expert dysmorphism score. However, in some patients, different dysmorphism aspects were captured making the metrics potentially complementary. The computational dysmorphism and asymmetry scores both enhanced the individual expert dysmorphism scores in differentiating Mendelian from non-Mendelian cases. Furthermore, the computational asymmetry score enhanced the average expert opinion in predicting a Mendelian cause. By design, our study does not allow to draw conclusions on the actual point-of-care use of 3D facial analysis. Nevertheless, 3D morphometric analysis is promising for developing clinical dysmorphology applications in diagnostics and training.<br /> (© 2024 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1399-0004
Volume :
106
Issue :
5
Database :
MEDLINE
Journal :
Clinical genetics
Publication Type :
Academic Journal
Accession number :
39056288
Full Text :
https://doi.org/10.1111/cge.14595