An automatic facial landmarking for children with rare diseases

Author:

Hennocq Quentin12ORCID,Bongibault Thomas1,Bizière Matthieu1,Delassus Ombline1,Douillet Maxime1,Cormier‐Daire Valérie3,Amiel Jeanne3,Lyonnet Stanislas3,Marlin Sandrine3,Rio Marlène3,Picard Arnaud2,Khonsari Roman Hossein2,Garcelon Nicolas1

Affiliation:

1. Imagine Institute, INSERM UMR 1163 Paris France

2. Département de chirurgie maxillo‐faciale et chirurgie plastique pédiatrique Hôpital Necker – Enfants Malades, Assistance Publique – Hôpitaux de Paris, Centre de Référence des Malformations Rares de la Face et de la Cavité Buccale MAFACE, Filière Maladies Rares TeteCou, Faculté de Médecine, Université de Paris Cité Paris France

3. Fédération de médecine génomique Hôpital Necker – Enfants Malades, Assistance Publique – Hôpitaux de Paris, Faculté de Médecine, Université de Paris Cité Paris France

Abstract

AbstractTwo to three thousand syndromes modify facial features: their screening requires the eye of an expert in dysmorphology. A widely used tool in shape characterization is geometric morphometrics based on landmarks, which are precise and reproducible anatomical points. Landmark positioning is user dependent and time consuming. Many automatic landmarking tools are currently available but do not work for children, because they have mainly been trained using photographic databases of healthy adults. Here, we developed a method for building an automatic landmarking pipeline for frontal and lateral facial photographs as well as photographs of external ears. We evaluated the algorithm on patients diagnosed with Treacher Collins (TC) syndrome as it is the most frequent mandibulofacial dysostosis in humans and is clinically recognizable although highly variable in severity. We extracted photographs from the photographic database of the maxillofacial surgery and plastic surgery department of Hôpital Necker–Enfants Malades in Paris, France with the diagnosis of TC syndrome. The control group was built from children admitted for craniofacial trauma or skin lesions. After testing two methods of object detection by bounding boxes, a Haar Cascade‐based tool and a Faster Region‐based Convolutional Neural Network (Faster R‐CNN)‐based tool, we evaluated three different automatic annotation algorithms: the patch‐based active appearance model (AAM), the holistic AAM, and the constrained local model (CLM). The final error corresponding to the distance between the points placed by automatic annotation and those placed by manual annotation was reported. We included, respectively, 1664, 2044, and 1375 manually annotated frontal, profile, and ear photographs. Object recognition was optimized with the Faster R‐CNN‐based detector. The best annotation model was the patch‐based AAM (p < 0.001 for frontal faces, p = 0.082 for profile faces and p < 0.001 for ears). This automatic annotation model resulted in the same classification performance as manually annotated data. Pretraining on public photographs did not improve the performance of the model. We defined a pipeline to create automatic annotation models adapted to faces with congenital anomalies, an essential prerequisite for research in dysmorphology.

Funder

Agence Nationale de la Recherche

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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