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

Author:

Sleyp Yoeri1,Matthews Harold S.123,Vanneste Michiel14,Vandenhove Laura1,Delanote Valentine4,Hoskens Hanne12,Indencleef Karlijne12,Teule Hanne4,Larmuseau Maarten H. D.156,Steyaert Jean78,Devriendt Koenraad14,Claes Peter1239,Peeters Hilde148

Affiliation:

1. Department of Human Genetics KU Leuven Leuven Belgium

2. Medical Imaging Research Center UZ Leuven Leuven Belgium

3. Facial Sciences Research Group Murdoch Children's Research Institute Parkville Victoria Australia

4. Center for Human Genetics University Hospitals Leuven Leuven Belgium

5. Antwerp Cultural Heritage Sciences, ARCHES UAntwerpen Antwerpen Belgium

6. Histories vzw Ghent Belgium

7. Center for Developmental Psychiatry KU Leuven Leuven Belgium

8. Leuven Autism Research (LAuRes) KU Leuven Leuven Belgium

9. Department of Electrical Engineering, ESAT/PSI KU Leuven Leuven Belgium

Abstract

AbstractRecognizing 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.

Publisher

Wiley

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