Characterization of dental phenotypes and treatment modalities in Korean patients with Parry–Romberg syndrome
10.4041/kjod.2020.50.6.407
- Author:
Sun jin YIM
1
;
Il-Hyung YANG
;
Seung-Hak BAEK
Author Information
1. Department of Orthodontics, School of Dentistry, Seoul National University, Seoul, Korea
- Publication Type:Original Article
- From:The Korean Journal of Orthodontics
2020;50(6):407-417
- CountryRepublic of Korea
- Language:English
-
Abstract:
Objective:To investigate the dental phenotypes and treatment modalities (TxMod) in Korean patients with Parry–Romberg syndrome (PRS) using longitudinal data.
Methods:The samples consisted of 10 PRS patients, who were treated and/or followed-up at Seoul National University Dental Hospital between 1998 and 2019. Using a novel PRS severity index based on the numbers of the atrophy-involved area and asymmetry-involved item, we classified them into mild (n = 3), moderate (n = 2), and severe (n = 5). Dental phenotypes, including congenitally missing tooth (Con-Missing-Tooth), microdontia, tooth with short root (Short-Root), tooth with dilacerated root, and delayed eruption/impacted tooth, were investigated along with Tx-Mod.
Results:The side of occurrence of all dental phenotypes showed 100% concordance with the side of PRS involvement. The most two common dental phenotypes were Con-MissingTooth and Short-Root (n = 29 and n = 17 in six patients). The sums of the average number of Con-Missing-Tooth and Short-Root increased from mild PRS to moderate PRS and severe PRS cases (1.0, 6.0, and 6.2). In terms of TxMod, growth observation due to mild atrophy, fixed orthodontic treatment, and grafting were used for mild PRS cases. Tx-Mod for moderate PRS cases involved growth observation for surgery due to an early age at the initial visit. For severe PRS cases, diverse Tx-Mod combinations including unilateral functional appliance, fixed orthodontic treatment, growth observation, grafting, and orthognathic surgery were used.
Conclusions:The novel PRS severity index may be useful to provide primary data for individualized diagnosis and treatment planning for PRS patients.
