Evidence map›Paper›PMID 42661064›Full record

ArticleEuropean journal of human genetics : EJHG2026

Utility of Face2Gene's DeepGestalt and D-Score applications in paediatric neurodevelopmental disorders in South Africa.

Zandrè Bruwer, Hendrike Mc Donald, Michal R Zieff, Emma Eastman, Brigitte Melly, Rizqa Sulaiman-Bardien, Karen Fieggen, Shahida Moosa, Emily O'Heir, Christina Austin Tse and 9 more

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Article in European journal of human genetics : EJHG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Zandrè Bruwer *Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital and University of Cape Town, Observatory, Cape Town, South Africa. zandrebruwer@gmail.com.ORCID http://orcid.org/0000-0002-6594-2512
Hendrike Mc Donald *Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital and University of Cape Town, Observatory, Cape Town, South Africa.
Michal R ZieffDepartment of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital and University of Cape Town, Observatory, Cape Town, South Africa.
Emma EastmanDepartment of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital and University of Cape Town, Observatory, Cape Town, South Africa.
Brigitte MellyDepartment of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital and University of Cape Town, Observatory, Cape Town, South Africa.
Rizqa Sulaiman-BardienDepartment of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital and University of Cape Town, Observatory, Cape Town, South Africa.ORCID http://orcid.org/0009-0004-4962-265X
Karen FieggenDivision of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.ORCID http://orcid.org/0000-0002-2910-6306
Shahida MoosaDivision of Molecular Biology and Human Genetics, Stellenbosch University, Stellenbosch, South Africa.ORCID http://orcid.org/0000-0002-4463-3067
Emily O'HeirThe Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-7669-8239
Christina Austin TseThe Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Ikeoluwa Osei-OwusuThe Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Alice GalvinThe Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-4831-5971
Celia van der MerweThe Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Anne O'Donnell-LuriaThe Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-6418-9592
Charles R NewtonNeuroscience Unit, KEMRI-Wellcome Trust, Center for Geographic Medicine Research Coast, Kilifi, Kenya.
Amina AbubakarNeuroscience Unit, KEMRI-Wellcome Trust, Center for Geographic Medicine Research Coast, Kilifi, Kenya.
Elise B RobinsonThe Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Kirsten A DonaldDepartment of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital and University of Cape Town, Observatory, Cape Town, South Africa.
NeuroDev Consortium

Funding

Joint Center for Mendelian GenomicsUM1HG008900 · NHGRI · BROAD INSTITUTE, INC. · PI O'DONNELL-LURIA, ANNE, REHM, HEIDI L · 2016 to 2020
$16.5M
Rare genetic disorders in NeuroDev: Insight into the genetic and phenotypic heterogeneity of ID, ASD and ADHD in South African PopulationsU01MH119689 · NIMH · BROAD INSTITUTE, INC. · PI DONALD, KIRSTY, O'DONNELL-LURIA, ANNE · 2019 to 2023
$5.2M
A powerful web-based discovery platform for rare disease geneticsR01HG009141 · NHGRI · BROAD INSTITUTE, INC. · PI QUINLAN, AARON R, REHM, HEIDI L · 2017 to 2020
$2.9M
Broad Institute | Stanley Center for Psychiatric Research, Broad Institute (Stanley Center) 599648U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) R01 HG009141U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) UM1 HG008900U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) U01MH119689
6 · The paper itself

Abstract

Face2Gene is a clinical tool that leverages facial features to aid genetic diagnosis. The DeepGestalt application suggests potential diagnoses based on facial similarity, while the D-Score evaluates likelihood of an individual having dysmorphic features suggestive of a possible genetic diagnosis. Given performance variability across populations and limited data from South Africa, this study assessed clinical utility in South African children with neurodevelopmental disorders (NDDs). Facial photographs from 301 children were analysed. The cohort comprised three groups: 36 children with NDDs with confirmed molecular diagnoses, 176 with NDDs without molecular diagnoses and 89 unaffected children. Diagnostic (recognition) accuracy was measured by whether the confirmed diagnosis appeared in the top-1 or top-10 ranked algorithm-generated suggestions (DeepGestalt). D-Scores were extracted to calculate group differences. Among children with confirmed molecular diagnoses, accuracy was 19% (95% CI: 9-35%) (top-1) and 34% (95% CI: 20-52%) (top-10), improving to 33% (95% CI: 16-56%) and 61% (95% CI: 39-80%) when limited to conditions included in the DeepGestalt training set. One-way ANOVA revealed differences between participants with and without significant dysmorphic features, as assessed by clinicians. The D-Score demonstrated moderate sensitivity (78%, [95% CI: 0.64, 0.88]) and low specificity (42%, [95% CI: 0.38, 0.50]), but high negative predictive value (91%, [95% CI: 0.84, 0.95]), suggesting it may be more useful for ruling out dysmorphism; however, the low specificity indicates a high rate of false positives, even among clinically non-dysmorphic children. These findings suggest that under-representation of African populations may limit clinical performance and equity of AI-based facial phenotyping tools.

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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.