Evidence map›Paper›PMID 37664547›Full record

ArticleFrontiers in pediatrics2023

AI-based diagnosis in mandibulofacial dysostosis with microcephaly using external ear shapes.

Quentin Hennocq, Thomas Bongibault, Sandrine Marlin, Jeanne Amiel, Tania Attie-Bitach, Geneviève Baujat, Lucile Boutaud, Georges Carpentier, Pierre Corre, Françoise Denoyelle and 14 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Prenatal Ultrasound and Genetic Diagnosis ofThe application of clinical genetics · 2026
    Article
  5. Review
  6. Humanitarian Facial Recognition for Rare Craniofacial Malformations.Plastic and reconstructive surgery. Global open · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 10 institutions in 4 countries.

Quentin HennocqImagine Institute, INSERM UMR1163, Paris, France.
Thomas BongibaultImagine Institute, INSERM UMR1163, Paris, France.
Sandrine MarlinImagine Institute, INSERM UMR1163, Paris, France.
Jeanne AmielImagine Institute, INSERM UMR1163, Paris, France.
Tania Attie-BitachImagine Institute, INSERM UMR1163, Paris, France.
Geneviève BaujatImagine Institute, INSERM UMR1163, Paris, France.
Lucile BoutaudService de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine, Université de Paris Cité, Paris, France.
Georges CarpentierCHU Lille, Inserm, Service de Chirurgie Maxillo-Faciale et Stomatologie, U1008-Controlled Drug Delivery Systems and Biomaterial, Université de Lille, Lille, France.
Pierre CorreDepartment of Oral and Maxillofacial Surgery, INSERM U1229-Regenerative Medicine and Skeleton RMeS, Nantes, France.
Françoise DenoyelleDepartment of Paediatric Otolaryngology, AP-HP, Hôpital Necker-Enfants Malades, Paris, France.
François Djate DelbrahImagine Institute, INSERM UMR1163, Paris, France.
Maxime DouilletImagine Institute, INSERM UMR1163, Paris, France.
Eva GallianiService de Chirurgie Maxillo-Faciale et Chirurgie Plastique, 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.
Wuttichart KamolvisitCenter of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Stanislas LyonnetImagine Institute, INSERM UMR1163, Paris, France.
Dan MileaDuke-NUS Medical School Singapore, Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
Véronique PingaultImagine Institute, INSERM UMR1163, Paris, France.
Thantrira PorntaveetusCenter of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Sandrine Touzet-RoumazeilleCHU Lille, Inserm, Service de Chirurgie Maxillo-Faciale et Stomatologie, U1008-Controlled Drug Delivery Systems and Biomaterial, Université de Lille, Lille, France.
Marjolaine WillemsDépartement de Génétique Clinique, CHRU de Montpellier, Hôpital Arnaud de Villeneuve, Institute for Neurosciences of Montpellier, INSERM, Univ Montpellier, Montpellier, France.
Arnaud PicardService de Chirurgie Maxillo-Faciale et Chirurgie Plastique, 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.
Marlène RioImagine Institute, INSERM UMR1163, Paris, France.
Nicolas GarcelonImagine Institute, INSERM UMR1163, Paris, France.
Roman H KhonsariImagine Institute, INSERM UMR1163, Paris, France.
Institut des Maladies Génétiques Imagine · FRAssistance Publique – Hôpitaux de Paris · FRUniversité Paris Cité · FRCentre Hospitalier Universitaire de Nantes · FRChulalongkorn University · THInserm · FRBiomatériaux et Bioingénierie · FRHôpital Saint Eloi · FRSingapore National Eye Center · SGUniversité de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Mandibulo-Facial Dysostosis with Microcephaly (MFDM) is a rare disease with a broad spectrum of symptoms, characterized by zygomatic and mandibular hypoplasia, microcephaly, and ear abnormalities. Here, we aimed at describing the external ear phenotype of MFDM patients, and train an Artificial Intelligence (AI)-based model to differentiate MFDM ears from non-syndromic control ears (binary classification), and from ears of the main differential diagnoses of this condition (multi-class classification): Treacher Collins (TC), Nager (NAFD) and CHARGE syndromes. Methods: The training set contained 1,592 ear photographs, corresponding to 550 patients. We extracted 48 patients completely independent of the training set, with only one photograph per ear per patient. After a CNN-(Convolutional Neural Network) based ear detection, the images were automatically landmarked. Generalized Procrustes Analysis was then performed, along with a dimension reduction using PCA (Principal Component Analysis). The principal components were used as inputs in an eXtreme Gradient Boosting (XGBoost) model, optimized using a 5-fold cross-validation. Finally, the model was tested on an independent validation set. Results: We trained the model on 1,592 ear photographs, corresponding to 1,296 control ears, 105 MFDM, 33 NAFD, 70 TC and 88 CHARGE syndrome ears. The model detected MFDM with an accuracy of 0.969 [0.838-0.999] ( Conclusion: This is the first AI-based syndrome detection model in dysmorphology based on the external ear, opening promising clinical applications both for local care and referral, and for expert centers.

Indexed as

AIcraniofacial malformationdysmorphologymachine learningMFDM

Identifiers

PMID37664547
PMCPMC10469912
OpenAlexW4385982753

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.