ArticleInternational journal of environmental research and public health2024
Oral Health-Related Quality of Life in Rare Disorders of Congenital Facial Weakness.
Denise K Liberton, Konstantinia Almpani, Rashmi Mishra, Carol Bassim, Carol Van Ryzin, On Behalf Of The Moebius Syndrome Research Consortium, Bryn D Webb, Ethylin Wang Jabs, Elizabeth C Engle, Francis S Collins and 2 more
Article in International journal of environmental research and public health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it
What it found
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2 · The registry
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
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5 · Who and what money
Authors and funding
12 authors.
Denise K LibertonCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.
Konstantinia AlmpaniCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0001-7558-6796
Rashmi MishraDepartment of Orofacial Sciences, School of Dentistry, University of California, San Francisco, CA 94143, USA.
Carol BassimCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.
Carol Van RyzinMetabolic Medicine Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
On Behalf Of The Moebius Syndrome Research Consortium
Bryn D WebbDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Ethylin Wang JabsDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Elizabeth C EngleDepartments of Neurology and Ophthalmology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0001-8194-7738
Francis S CollinsCenter for Precision Health Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-1023-7410
Irini ManoliMetabolic Medicine Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0003-1543-2941
Janice S LeeCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.
Funding
Craniofacial Anomalies and RegenerationZIADE000746 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI LEE, JANICE · 2015 to 2025
$12.3M
Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI SCOTT Loren POMEROY, MUSTAFA SAHIN · 2021 to 2026
$9.4M
Genetics of Moebius syndrome and other congenital facial weakness disordersZIAHG200389 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI COLLINS, FRANCIS S. · 2013 to 2024
$4.9M
Birth Defects: Moebius syndrome and related facial weakness disordersU01HD079068 · NICHD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BROOKS, BRIAN PATRICK, ENGLE, ELIZABETH C. · 2014 to 2016
$1.1M
Intramural NIH HHS ZIA DE000746Intramural NIH HHS ZIA HG200389Intramural Research Program of the National Institute of Dental and Craniofacial Research; National Human Genome Research Institute; Intramural-extramural collaborative grant 1ZIADE000746, PI: Janice Lee; ZIAHG200389, PI: Francis S. Collins; U01HD079068, Intramural PIs: Irini Manoli, Brian Brooks, Carlo Pierpaoli, Extramural PIs: Ethylin Wang Jabs and Elizabeth Engle.NICHD NIH HHS P50 HD105351NICHD NIH HHS U01 HD079068
6 · The paper itself
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,
Indexed as
Oral HealthQuality of LifeAdolescentAdultCase-Control StudiesChildFacial ParalysisFemaleHumansMaleMiddle AgedRare DiseasesYoung AdultCarey Fineman Ziter syndromecongenital fibrosis of the extraocular musclesfacial weakness disordershereditary congenital facial palsymoebius syndromeOHIP-14OHRQoLOral Health Impact Profilesmile surgery
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.
Oral Health-Related Quality of Life in Rare Disorders of Congenital Facial Weakness. · full record | OpenQuestion