Inclusion criteria: |
- Chronic and stable unilateral peripheral facial paresis, i.e., more than one year since the onset of the symptom, whatever its cause |
- Age ≥ 18 |
- Outpatient |
- Sufficient motivation level to participate in a 6-month facial rehabilitation program, based on the opinion of the investigator |
- Signed consent |
- Medically insured |
Exclusion criteria: |
- Evolving tumor causing the peripheral facial paresis |
- Facial botulinum toxin injection less than six months before enrollment in the study, or planned during the study period |
- Facial surgery less than two years before enrollment into the study or planned during the study period |
- V-VII or XII-VII anastomosis or muscle transfer prior to enrollment into the study or planned during the study |
- Nonsurgical aesthetic treatments – hyaluronic acid / lipofilling / laser / tensor thread – less than two years before enrollment in the study or planned during the study period |
- Recurrent facial paresis |
- Participation in another interventional research protocol on the face (aesthetic, rehabilitative, or surgical) |
- Intercurrent disorder that could hinder the ability to participate in the rehabilitation program |
- Preexisting cognitive, mental or psychological disorder preventing participation in the rehabilitation program or in the follow-up assessments, based on the opinion of the investigator |
- Patient under legal protection |