Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Dental phenotype in Crouzon syndrome: A controlled radiographic study in 22 patients.

Archives of oral biology - 1 Nov 2021

Sicard Ludovic, Hennocq Quentin, Paternoster Giovanna, Arnaud Eric, Dure-Molla Muriel de la, Khonsari Roman Hossein

Abstract excerpt

OBJECTIVE: This retrospective radiographic controlled study investigates the dental phenotype in patients with Crouzon syndrome to determine if differences are observed as suggested by the FGFR2C342Y/+ Crouzon mouse models, and whether these models could be of interest to study the role of this mutation in tooth development. DESIGN: We assessed dental phenotype using dedicated linear measurements in 22 children...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Craniofacial Dysostosis
Share to Disease Models, Animal

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation

Share to Phenotype

Source

Identifiers

PMID: 34500259
DOI: 10.1016/j.archoralbio.2021.105253

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Dental phenotype in Crouzon syndrome: A controlled radiographic study in 22 patients.PMID 34500259Read ↗

Extensive phenotyping of the orofacial and dental complex in Crouzon syndrome.Semantic proximity Read ↗

The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT.Semantic proximity Read ↗

Dental phenomics: advancing genotype to phenotype correlations in craniofacial research.Semantic proximity Read ↗

Tissue-specific responses to aberrant FGF signaling in complex head phenotypes.Semantic proximity Read ↗

Teeth anomalies and genetics, including genetic syndromesSemantic proximity Read ↗

Contributing Factors for Angle's Class III Phenotype in Crouzon Syndrome.Semantic proximity Read ↗

Alterations in Tooth Structure and Associated Systemic Conditions.Semantic proximity Read ↗

Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentitionSemantic proximity Read ↗

The Fgfr2 W290R mouse model of Crouzon syndrome.Semantic proximity Read ↗

Crouzon syndrome with bony upper airway obstruction: case report and review literature.Semantic proximity Read ↗

Genetic studies of craniofacial anomalies: clinical implications and applications.Semantic proximity Read ↗

Anomalies of the Primary Dentition in Patients with Oculo-Facio-Cardio-Dental (OFCD) SyndromeSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.