Evidence map›Paper›PMID 40987814›Full record

ArticleEuropean journal of human genetics : EJHG2025

Expanding the molecular spectrum of aggrecanopathies: exploring 24 patients with ACAN significant variants.

Melek Trigui, Nathalie Pallares-Ruiz, David Geneviève, Cyril Amouroux, Thomas Edouard, Sabine Sigaudy, Marjolaine Willems, Mouna Barat-Houari

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2026
    Article
  2. Article
  3. Review
  4. Genetic Heterogeneity Underlying Familial Short Stature.Diagnostics (Basel, Switzerland) · 2025
    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

8 authors.

Melek TriguiDepartment of Molecular Genetics and Cytogenomics, Rare and Auto Inflammatory Diseases Unit, CHU Montpellier, Montpellier, France. melektrigui2018@gmail.com.ORCID 0009-0004-2101-8880
Nathalie Pallares-RuizDepartment of Molecular Genetics and Cytogenomics, Rare and Auto Inflammatory Diseases Unit, CHU Montpellier, Montpellier, France. n-ruiz@chu-montpellier.fr.ORCID 0009-0003-6021-8028
David GenevièveReference Centre AD SOOR, AnDDI-RARE, Reference Centre for Rare Skeletal Disorders, OSCAR Network, Department of Medical Genetics, Rare diseases and Personalized medicine, CHU Montpellier, University of Montpellier, Montpellier, France. d-genevieve@chu-montpellier.fr.ORCID 0000-0001-6928-6287
Cyril AmourouxNephrology and Endocrinology Unit, Multidisciplinary Pediatrics Department, OSCAR Network, Montpellier University Hospital. Education Department, School of Medicine, University of Montpellier, Arnaud de Villeneuve Hospital, Montpellier, France. cyril-amouroux@chu-montpellier.fr.ORCID 0000-0003-4251-6825
Thomas EdouardEndocrine, Bone Diseases and Genetics Unit, Reference Centre for Rare Diseases of Calcium and Phosphate Metabolism, OSCAR Network, ERN BOND, Children's Hospital, Toulouse University Hospital; RESTORE, INSERM U1301, Paul Sabatier University, Toulouse, France. edouard.t@chu-toulouse.fr.ORCID 0000-0002-9222-5009
Sabine SigaudyDépartement de Génétique Médicale, Hôpital Timone Enfant, Marseille, France. sabine.sigaudy@ap-hm.fr.
Marjolaine Willems *Reference Centre AD SOOR, AnDDI-RARE, Reference Centre for Rare Skeletal Disorders, OSCAR Network, Department of Medical Genetics, Rare diseases and Personalized medicine, CHU Montpellier, University of Montpellier, Montpellier, France. m-willems@chu-montpellier.fr.ORCID 0000-0002-2959-0935
Mouna Barat-Houari *Department of Molecular Genetics and Cytogenomics, Rare and Auto Inflammatory Diseases Unit, CHU Montpellier, Montpellier, France. mouna-barat@chu-montpellier.fr.ORCID 0000-0002-6712-0053

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Short stature is a prevalent clinical manifestation in children. While certain causes of short stature can be readily identifiable through routine biological tests, often physicians struggle to ascertain any underlying pathogenic cause, resulting in the diagnosis of idiopathic short stature (ISS). Aggrecan, encoded by ACAN, plays a crucial role in cartilage function and bone growth. The aim of our study is to establish a genotype-phenotype correlation in 24 patients carrying distinct ACAN variants. We conducted a panel-based analysis, including 82 genes associated with genetic skeletal disorders and/or short stature, in 388 French patients who consulted for short stature and/or or skeletal features. Genotype-phenotype correlation analysis was performed for all included subjects. Of all positive patients, 24 (≃20%) were found to carry pathogenic or likely pathogenic ACAN variants distributed across the gene, 20 of which had not been previously reported. We report 23 heterozygous cases and one original case with a homozygous SNV. Two patients harboured the same novel nonsense variant, yet exhibited different phenotypes. Familial studies performed in 21 families demonstrated that ACAN variants were inherited in 20 cases. The cohort demonstrated marked phenotypic heterogeneity, even among affected members within the same family. Radiological skeletal abnormalities were observed in 66% of patients. A comprehensive genomic approach is crucial to identify the true proportion of ISS with a monogenic condition. Our results expand the number of pathogenic ACAN variants with their associated phenotypic spectrum. Aggrecanopathies are heterogeneous and particularly frequent in apparently ISS, even without overt skeletal dysplasia.

Indexed as

AggrecansDwarfismAdolescentAdultChildChild, PreschoolFemaleHumansMaleMutationPedigreePhenotypeACAN protein, humanAggrecans

Identifiers

PMID40987814
PMCPMC12669688

What OpenQuestion holds

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Registered trials

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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.