Oral Health-Related Quality of Life in Rare Disorders of Congenital Facial Weakness

Author:

Liberton Denise K.1,Almpani Konstantinia1ORCID,Mishra Rashmi2,Bassim Carol1,Van Ryzin Carol3, ,Webb Bryn D.45,Jabs Ethylin Wang46,Engle Elizabeth C.789ORCID,Collins Francis S.10ORCID,Manoli Irini3ORCID,Lee Janice S.1

Affiliation:

1. Craniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA

2. Department of Orofacial Sciences, School of Dentistry, University of California, San Francisco, CA 94143, USA

3. Metabolic Medicine Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA

4. Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA

5. Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI 53705, USA

6. Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55902, USA

7. Departments of Neurology and Ophthalmology, Boston Children’s Hospital, Boston, MA 02115, USA

8. Departments of Neurology and Ophthalmology, Harvard Medical School, Boston, MA 02115, USA

9. Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA

10. Center for Precision Health Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA

Abstract

Congenital facial weakness (CFW) encompasses a heterogenous set of rare disorders presenting with decreased facial movement from birth, secondary to impaired function of the facial musculature. The aim of the present study is to provide an analysis of subject-reported oral health-related quality of life (OHRQoL) in congenital facial weakness (CFW) disorders. Forty-four subjects with CFW and age- and sex- matched controls were enrolled in an Institutional Review Board (IRB)-approved study. Demographic data, medical and surgical history, comprehensive oral examination, and the Oral Health Impact Profile (OHIP-14) were obtained. Compared to unaffected controls, subjects with CFW had higher OHIP-14 scores overall (mean ± SD: 13.11 ± 8.11 vs. 4.46 ± 4.98, p < 0.0001) and within five of seven oral health domains, indicating decreased OHRQoL. Although subjects with Moebius syndrome (MBS) were noted to have higher OHIP-14 scores than those with Hereditary Congenital Facial Paresis (HCFP), there was no significant correlation in OHIP-14 score to age, sex, or specific diagnosis. An increase in OHIP-14 scores in subjects was detected in those who had undergone reanimation surgery. In conclusion, subjects with CFW had poorer OHRQoL compared to controls, and subjects with MBS had poorer OHRQoL than subjects with HCFP. This study provides better understanding of oral health care needs and quality of life in a CFW cohort and suggests that guidelines for dental treatment are required.

Funder

Intramural Research Program of the National Institute of Dental and Craniofacial Research

National Human Genome Research Institute

intramural-extramural collaborative grant

Publisher

MDPI AG

Reference50 articles.

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