Evidence map›Paper›PMID 42277781›Full record

ArticleBMC pediatrics2026

Mandibular trabecular microarchitecture as a radiographic biomarker of bone health in children with 22q11.2 deletion syndrome.

Tulin Tasdemir, Melek Tassoker

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Article in BMC pediatrics, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Tulin TasdemirFaculty of Dentistry, Department of Pediatric Dentistry, Nigde Omer Halisdemir University, Nigde, 51240, Turkey. dt.tulintasdemir@gmail.com.ORCID 0000-0003-4884-4715
Melek TassokerFaculty of Dentistry, Department of Dentomaxillofacial Radiology, Necmettin Erbakan University, Konya, Meram, 42050, Turkey.ORCID 0000-0003-2062-5713

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDiGeorge Syndrome (DGS), or 22q11.2 deletion syndrome, is a multisystem genetic disorder characterized by distinct craniofacial features and profound endocrine alterations, particularly parathyroid dysfunction and chronic hypocalcemia. This study aimed to non-invasively evaluate the microarchitecture of mandibular trabecular bone in pediatric patients with DGS using fractal dimension (FD) analysis on panoramic radiographs, aiming to better understand the localized radiographic impact of systemic calcium dysregulation and its implications for clinical management. MATERIALS AND

methodsEleven pediatric patients diagnosed with DGS and eleven healthy, age- and sex-matched controls were enrolled. FD values were calculated using the box-counting method via ImageJ software across specific mandibular regions, including the condylar, gonial, and interdental areas. To assess measurement reliability and potential bias, a within-subject comparison of the right and left region of interests (ROIs) was conducted using the Wilcoxon signed-rank test. Regional influences of age and gender were evaluated using Spearman's correlation and Mann-Whitney U tests.

resultsA statistically significant reduction in trabecular complexity was identified in the right condylar region of the DGS group (p = 0.005). No significant differences were observed between the right and left corresponding ROIs (p > 0.05), indicating an absence of measurement bias. While gender did not influence FD values, a localized moderate negative correlation was found between age and FD specifically in the left gonial region (r =-0.427, p = 0.047).

conclusionsThe reduction in localized mandibular trabecular complexity in children with DGS serves as a localized radiographic biomarker of the syndrome's underlying endocrine and calcium signaling disruptions. Safely managing the complex dentofacial needs of this vulnerable population requires a paradigm shift from isolated dental care to a closely coordinated, interdisciplinary approach involving pediatric endocrinologists, pediatricians, and pediatric dentists.

Indexed as

Cancellous BoneDiGeorge SyndromeMandibleRadiography, PanoramicAdolescentBiomarkersCase-Control StudiesChildChild, PreschoolFemaleFractalsHumansMaleBiomarkers22q11.2 deletion syndromeBone microarchitectureDiGeorge syndromeFractal analysisPanoramic radiographyPediatric endocrinology

Identifiers

PMID42277781
PMCPMC13393614

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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.