About this trial
Some sparse scientific data support the hypothesis that otherwise unexplained emphysema may be associated with FLNA variants. This transversal multicentric study aimed to describe the frequency of emphysema in patients carrying an FLNA variation. Patients with FLNA variations who accept the study will benefit from a chest physician's clinical examination, respiratory function tests, a cardiac ultrasound and a chest scan. The primary endpoint is to describe emphysema's frequency in patients carrying FLNA variation. The other objectives are to describe emphysema's features in these patients, the prevalence of pulmonary hypertension and to describe their lung function abnormalities. The final goal is to confirm the association between unexplained emphysema and FLNA mutation.
Eligibility criteria
Qualifiers
Patient with an FLNA mutation (or gene alteration)
Patient who has given written consent to participate in the trial
Socially insured patient
Patient willing to comply with all study procedures and duration
Disqualifiers
Patient refused or unable to give informed consent
Administrative reasons: inability to receive information, inability to participate in the entire study, lack of coverage by the social security system,
Pregnant or breastfeeding women
Patient under guardianship
Trial design
Treatments tested in this trial
- Radiation: Chest HRCT