Loading…

A Proposal for the Classification of Temporomandibular Joint Disc Deformity in Hemifacial Microsomia

Hemifacial microsomia (HFM) is the second most common congenital craniofacial disease and has a wide spectrum of symptoms. The classic diagnostic criterion for hemifacial microsomia is the OMENS system, which was later refined to the OMENS+ system to include more anomalies. We analyzed the data of 1...

Full description

Saved in:
Bibliographic Details
Published in:Bioengineering (Basel) 2023-05, Vol.10 (5), p.595
Main Authors: Xue, Xiaochen, Liu, Zhixu, Wei, Hongpu, Wang, Xudong
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Hemifacial microsomia (HFM) is the second most common congenital craniofacial disease and has a wide spectrum of symptoms. The classic diagnostic criterion for hemifacial microsomia is the OMENS system, which was later refined to the OMENS+ system to include more anomalies. We analyzed the data of 103 HFM patients with magnetic resonance imaging (MRI) for temporomandibular joint (TMJ) discs. The TMJ disc classification was defined into four types: D0 for normal disc size and shape; D1 for disc malformation with adequate length to cover the (reconstructed) condyle; D2 for disc malformation with inadequate length to cover the (reconstructed) condyle; and D3 for no obvious presence of a disc. Additionally, this disc classification was positively correlated with the mandible classification (correlation coefficient: 0.614, < 0.01), ear classification (correlation coefficient: 0.242, < 0.05), soft tissue classification (correlation coefficient: 0.291, < 0.01), and facial cleft classification (correlation coefficient: 0.320, < 0.01). In this study, an OMENS+D diagnostic criterion is proposed, confirming the conjecture that the development of the mandibular ramus, ear, soft tissue, and TMJ disc, as homologous and adjacent tissues, is affected to a similar degree in HFM patients.
ISSN:2306-5354
2306-5354
DOI:10.3390/bioengineering10050595