Clinical Oral Manifestations of Ehlers Danlos Syndrome
Research type
Research Study
Full title
Oral Manifestations of Ehlers-Danlos Syndromes; A Systematic Analysis
IRAS ID
303719
Contact name
James Scott
Contact email
Sponsor organisation
Sheffield Teaching Hospitals NHS Foundation Trust
Duration of Study in the UK
0 years, 11 months, 30 days
Research summary
Ehlers-Danlos Syndrome is an inherited genetic disorder affecting connective tissues of the body. It is widely accepted that individuals diagnosed with one of the fourteen known subtypes of Ehlers-Danlos syndrome (EDS) have a significantly lowered oral health-related quality of life (OHQOL) due to some of the characteristics of the disease. Whilst a number of previous papers have attempted to link clinical findings with OHQOL, they have lacked scientific rigour, either with oral investigations or with genetic clarification of the underlying EDS. This project will employ observational cross-section methodology to measure qualitative and quantitative clinical characteristics in two subtypes of EDS patients; vascular EDS (vEDS) and classic EDS (cEDS). These findings will further our understanding of the oral manifestations of this hereditary connective tissue disorder. They will help inform future guidelines for the management of oral healthcare of EDS patients.
REC name
Wales REC 3
REC reference
22/WA/0194
Date of REC Opinion
26 Jul 2022
REC opinion
Further Information Favourable Opinion