Observational Study of a Cohort of Patients With Hereditary Epidermolysis Bullosa

Centre Hospitalier Universitaire de Nice

Status: Completed

Conditions: Epidermolysis Bullosa

Treatments: Other: clinical exam

Study type: Observational

Funder types: Other

Identifiers

NCT04217538

19-ODONTO-01

Details and patient eligibility

About

Hereditary Epidermolysis Bullosa (EBH) are rare dermatologic diseases characterized by cutaneous and mucosa fragility. Oral manifestations of few small cohort have been published. The main objective of this multicentric cohort study first in Europe was to report the oral status of these patients that were consulted in the MRDRC of this disease in Nice (France), Toulouse (France) and Louvain (Belgium). Then a correlation between the oral characteristics and the EBH type will be made, in order to facilitate the management of patient care and the prevention program that can be established to improve their oral health.

Enrollment: 41 patients

Sex: All

Ages: 7 months to 78 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patient with EBH
• patient consent for examination and use the clinical data for publication purpose

Exclusion criteria

Trial design

41 participants in 1 patient group

EBH

Treatment:

Other: clinical exam