Evidence map›Paper›PMID 41805094›Full record

ArticleThe Journal of craniofacial surgery

The Identification of Beckwith-Wiedemann Syndrome Through Swap Disentangled Variational Autoencoder.

Tia Rijlaarsdam, Luke Smith, Alexander Rickart, Silvia Schievano, David Dunaway, Eppo Wolvius, Lara van de Lande, Simone Foti, Juling Ong

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Article in The Journal of craniofacial surgery. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Tia RijlaarsdamUniversity College London (UCL) Great Ormond Street Institute of Child Health, London, UK.
Luke SmithUniversity College London (UCL) Great Ormond Street Institute of Child Health, London, UK.
Alexander RickartUniversity College London (UCL) Great Ormond Street Institute of Child Health, London, UK.
Silvia SchievanoUniversity College London (UCL) Great Ormond Street Institute of Child Health, London, UK.
David DunawayUniversity College London (UCL) Great Ormond Street Institute of Child Health, London, UK.
Eppo WolviusDepartment of Oral and Maxillofacial Surgery, Erasmus Medical Center, Rotterdam, Netherlands.
Lara van de LandeDepartment of Oral and Maxillofacial Surgery, Erasmus Medical Center, Rotterdam, Netherlands.
Simone FotiWellcome/EPSRC Centre for Interventional and Surgical Sciences, University College London.
Juling OngUniversity College London (UCL) Great Ormond Street Institute of Child Health, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital syndromes with subtle changes in maxillofacial morphology can pose significant diagnostic challenges, wherein artificial intelligence holds great promise in aiding diagnosis through shape analysis. The authors applied the recently proposed Swap Disentangled Variational Autoencoder (SD-VAE) in diagnosis of Beckwith-Wiedemann syndrome (BWS). The SD-VAE model was trained on a data set primarily comprised of surface 3D head scans [stereophotogrammetry (3D SPG)], gathered using a 3dMD Head System (3dMD LLC). It was also trained on CT scans when available. A total of 72 syndromic scans were used belonging to 56 different BWS patients. Scans of head shapes were pre-processed and annotated with 68 anatomic landmarks. This aided in achieving uniformity between the scans and a template mesh, making a better comparison possible. The SD-VAE model outputs were then visualized in a 2-dimensional space and classified as 'BWS-patient' or 'control'. For each anatomic facial region, the performance of the classification model was evaluated. This allowed us to understand the classification accuracy for each anatomic region as well as calculate the sensitivity and specificity for each region. The model demonstrated perfect diagnostic accuracy for BWS on the test set, with the most characteristic regions being the chin, cheeks, zygoma, eyes, jaw, and supraorbital region. This paper demonstrates how SD-VAE can be applied to 3D head meshes, to quantify the characteristic features of BWS. The authors distinguished BWS-specific features from those of the general population with high diagnostic accuracy. This makes SD-VAE a promising tool for aiding the referral and diagnosis of BWS in the future.

Indexed as

AutoencoderBeckwith-Wiedemann SyndromeImaging, Three-DimensionalAnatomic LandmarksFemaleHumansPhotogrammetrySensitivity and SpecificityTomography, X-Ray Computed3D stereophotogrammetryartificial intelligenceautoencodersBeckwith-Wiedemann syndromedeep learning

Identifiers

PMID41805094
PMCPMC13290057

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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.