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DOI 10.1177/10556656251344128

Медицинская библиотека · The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association · 2025

Multimodality Craniofacial Phenotyping of Congenital Facial Weakness Disorders.

Almpani Konstantinia, Devine Katelin R, Liberton Denise K, Mishra Rashmi, Bassim Carol, Van Ryzin Carol, Facio Flavia M, Webb Bryn D, Barry Brenda J, Engle Elizabeth C, Wang Jabs Ethylin, Collins Francis S, Manoli Irini, Lee Janice S, Moebius Syndrome Research Consortium

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Аннотация

ObjectiveCongenital facial weakness (CFW) disorders are a heterogeneous group of rare conditions, that present at birth, with reduced facial movement, and mask-like facies. This study utilized a multimodality approach to examine the craniofacial and intraoral phenotypes among CFW disorders: Moebius syndrome (MBS), Hereditary Congenital Facial Palsy (HCFP), β-tubulin isotype 3 syndrome (CFEOM3A-TUBB3), Carey-Fineman-Ziter syndrome (CFZS), and a group of rarer disorders (Other).DesignProspective cohort study.

Setting

Dental clinic.

Participants

Sixty individuals (sex ratio 1:1, mean age 26.2 ± 17.5 years) with a diagnosis of CFW.Interventions: Deep clinical craniofacial and dental phenotyping, three-dimensional facial surface and cone-beam computed tomography scans, and cephalometric and geometric morphometric analyses.ResultsCFEOM3A-TUBB3, MBS, and CFZS groups had the highest prevalence of craniofacial anomalies; HCFP individuals were least affected. CFEOM3A-TUBB3 had a higher prevalence of short lower face (75%), poor oral hygiene (100%)/decay (75%), and Class II malocclusion (87.5%). Moebius syndrome was associated with lagophthalmos (90.9%), tongue fissures (72.4%), tight/small oral orifice (51.7%), and tongue fasciculations (50%). Carey-Fineman-Ziter syndrome had oblong facial shape (100%), downward lip commissures (100%), and abnormal hearing (60%). Moderate-severe decay/gingivitis correlated with restricted oral orifice, common among patients with facial animation/sling surgery. Morphologically, the CFW cohort had a relatively small craniofacial centroid size, anthropometric measurements, and distinct craniofacial shapes for each subtype.ConclusionsCongenital facial weakness can result in abnormal craniofacial development in addition to the loss of facial movement. Multimodality phenotypic characterization of CFW disorders elucidated key clinical findings and distinct craniofacial shape segregation among the different groups.

Для цитирования: Almpani Konstantinia, Devine Katelin R, Liberton Denise K, Mishra Rashmi, Bassim Carol, Van Ryzin Carol, Facio Flavia M, Webb Bryn D, Barry Brenda J, Engle Elizabeth C, Wang Jabs Ethylin, Collins Francis S, Manoli Irini, Lee Janice S, Moebius Syndrome Research Consortium. Multimodality Craniofacial Phenotyping of Congenital Facial Weakness Disorders.. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 2025. DOI: 10.1177/10556656251344128.

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