Evidence map›Paper›PMID 42443842›Full record

ArticleBMC pediatrics2026

Craniofacial features and pathogenic variants in 1,252 children with neurodevelopmental disorders.

Ran Chen, Dandan Wu, Jerry Zhang, Yanyan Dai, Dongqing Xia, Mengying Chen, Xiaonan Li, Qianqi Liu, Yinhua Chen, Rong Li

Abstract read
In one paragraph

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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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

10 authors.

Ran Chen *Child Healthcare Department, Children's Hospital of Nanjing Medical University, Jiangdong South No.8 Road, Nanjing, 210008, China.
Dandan Wu *Child Mental Health Department, Children's Hospital of Nanjing Medical University, Nanjing, China.
Jerry ZhangBasis International School Nanjing, Nanjing, Jiangsu, China.
Yanyan DaiChild Healthcare Department, Children's Hospital of Nanjing Medical University, Jiangdong South No.8 Road, Nanjing, 210008, China.
Dongqing XiaChild Healthcare Department, Children's Hospital of Nanjing Medical University, Jiangdong South No.8 Road, Nanjing, 210008, China.
Mengying ChenChild Healthcare Department, Children's Hospital of Nanjing Medical University, Jiangdong South No.8 Road, Nanjing, 210008, China.
Xiaonan LiChild Healthcare Department, Children's Hospital of Nanjing Medical University, Jiangdong South No.8 Road, Nanjing, 210008, China.
Qianqi LiuChild Healthcare Department, Children's Hospital of Nanjing Medical University, Jiangdong South No.8 Road, Nanjing, 210008, China.
Yinhua Chen *Nursing Department, Children's Hospital of Nanjing Medical University, Jiangdong South No.8 Road, Nanjing, Jiangsu, 210008, China. yimihua_ca@163.com.
Rong Li *Child Healthcare Department, Children's Hospital of Nanjing Medical University, Jiangdong South No.8 Road, Nanjing, 210008, China. 15850780062@163.com.ORCID 0009-0007-3919-0920

Funding

Jiangsu Medical Association Pediatric Medical Research Special Fund Project SYH-32034-0070Jiangsu Medical Association Scientific Research Special Fund SYH-32034-0097
6 · The paper itself

Abstract

objectiveNeurodevelopmental disorders (NDDs) are a group of highly heterogeneous diseases with complex genetic etiology. Craniofacial anomalies are frequently observed in children with NDDs. This study aimed to identify craniofacial features in children with NDDs for early warning of genetic NDDs.

methodsPeripheral blood samples were collected from children with NDDs and their parents for exome sequencing and copy number variation analysis. Typical clinical characteristics of children with NDDs, including craniofacial anomalies, limb malformations, and organ deformities, were thoroughly observed and recorded.

resultsAmong 1,252 children with NDDs, there were 283 cases with pathogenic variants and 219 cases of craniofacial abnormalities. The positive detection rate of pathogenic variants in the craniofacial anomaly group was significantly higher than that in the overall cohort and the cohort of non-craniofacial anomaly (P < 0.01). Eyes were the most common craniofacial region with anomalies in children with NDDs carrying pathogenic variants, followed by the head and oral cavity. Significant differences were observed in the rates of positive characteristics in the eight craniofacial regions between children with NDDs either carrying pathogenic variants or not. The craniofacial anomalies in ≥ 3 regions indicated a positive detection rate nearly 75% of pathogenic variants.

conclusionCraniofacial anomalies are highly predictive of pathogenic variants in children with NDDs. Moreover, the eyes, head and oral cavity are the most common craniofacial regions with anomalies in children with NDDs carrying pathogenic variants. For a definite diagnosis, genetic testing is recommended for children with unknown causes of NDDs and anomalies in three or more craniofacial regions.

Indexed as

Craniofacial AbnormalitiesNeurodevelopmental DisordersAdolescentChildChild, PreschoolDNA Copy Number VariationsExome SequencingFemaleHumansInfantMaleMutationCraniofacial anomaliesNeurodevelopmental disordersPathogenic variants

Identifiers

PMID42443842
PMCPMC13584260

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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.