Evidence map›Paper›PMID 41706026›Full record

ArticleClinical genetics2026

Craniofacial Dysmorphology Associated With Phelan-McDermid Syndrome Using Three-Dimensional Morphometrics.

Katherine Weisensee, Sara M Sarasua, Lior Rennert, Curtis Rogers, Katy Phelan, Kara Powder, Luigi Boccuto

Abstract read
In one paragraph

Article in Clinical genetics, 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
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0citing papers in PubMed
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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

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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

7 authors.

Katherine WeisenseeDepartment of Anthropology, Sociology, and Criminal Justice, Clemson University, Clemson, South Carolina, USA.
Sara M SarasuaSchool of Nursing, Clemson University, Clemson, South Carolina, USA.ORCID 0000-0002-1625-7404
Lior RennertDepartment of Public Health Sciences, Clemson University, Clemson, South Carolina, USA.
Curtis RogersGreenwood Genetic Center, Greenville, South Carolina, USA.
Katy PhelanFlorida Cancer Specialists & Research Institute, Fort Myers, Florida, USA.
Kara PowderDepartment of Biological Sciences, Clemson University, Clemson, South Carolina, USA.ORCID 0000-0001-7415-4262
Luigi BoccutoSchool of Nursing, Clemson University, Clemson, South Carolina, USA.

Funding

Tissue Structural and Neural Remodeling in Human Sacroiliac JointP20GM121342 · NIGMS · CLEMSON UNIVERSITY · PI Jeryl Jones · 2018 to 2026
$24.7M
Craniofacial Dysmorphology Associated with Phelan-McDermid Syndrome using Three-Dimensional MorphometricsR03DE027497 · NIDCR · CLEMSON UNIVERSITY · PI ROGERS, R CURTIS, WEISENSEE, KATHERINE · 2018 to 2019
$197k
College of Behavioral, Social, and Health Sciences Clemson UniversityNIDCR NIH HHS P20 GM121342NIDCR NIH HHS R03DE027497NIGMS NIH HHS P20 GM121342
6 · The paper itself

Abstract

Phelan-McDermid syndrome (PMS) frequently presents with distinctive facial features, although a typical facial phenotype for this condition has not been well characterized. Facial dysmorphology assessments can be subjective, depending on the experience and training of the clinical geneticist conducting the patient evaluation. In this investigation, we sought to quantitatively assess craniofacial features in Phelan-McDermid syndrome. Three-dimension (3D) morphometric assessment was conducted of 100 children and young adults diagnosed with PMS and 536 age- and sex-matched typically developing subjects obtained from the FaceBase consortium. The data were analyzed using principal component analysis (PCA), Procrustes MANOVA, and canonical variates analysis (CVA). We found that people with PMS aged 3-32 years have quantitatively distinctive craniofacial features compared to age- and sex-matched normed people. We observed an elongated face, a pointed chin, a flattened midface, and nasal expansion as characteristic of the PMS facial phenotype. Further, distinct growth patterns were observed, with children ages 3-6 and 7-12 years having more rapid growth compared to matched normed samples. While people with PMS have distinctive facial features, individual variation is the greatest contribution to facial variation. Quantitative assessment of craniofacial features paired with genotype can further our understanding of genetic contributions to craniofacial development.

Indexed as

Chromosome DisordersCraniofacial AbnormalitiesAdolescentAdultChildChild, PreschoolChromosome DeletionChromosomes, Human, Pair 22FaceFemaleHumansImaging, Three-DimensionalMalePhenotypePrincipal Component AnalysisYoung AdultdysmorphologyPhelan–McDermid syndrome: SHANK3three‐dimensional Morphometrics

Identifiers

PMID41706026
PMCPMC13167632

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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.