Autoinflammatory syndrome Turner syndrome Rare lung diseases Mutation Pulmonary fibrosis Classification Bronchiectasis Atherosclerosis Pulmonary hypertension Children Cohort TNFAIP3 ABCA3 COVID-19 France A20 haploinsufficiency Lipodystrophy Serum amyloid A TNFRSF1A Premature ovarian insufficiency CRISPR-Cas9 Rare diseases Karyotype NLRP3 AL amyloidosis TCF4 Surfactant Biomarkers Male infertility Biopsie Adolescent Familial Mediterranean fever Pituitary Situs inversus Maladies auto-inflammatoires Adipokines ICSI Pyrine Mortality Colchicine Infant Fibrose pulmonaire Intellectual disability Lung function Prognosis Mosaic Interleukine 1 Cytokines Osteosarcoma PCD NLRC4 TRAPS Phenotype Pregnancy Biopsy Pyrin Genetics Autoinflammation GHRHR Primary ciliary dyskinesia Vasculitis Idiopathic pulmonary fibrosis Humans AA amyloidosis MEFV Autoimmunity Management Autoinflammatory disease Paediatric interstitial lung disease Founder effect Genetic analysis Inflammasome Dynein Sarcoidosis NGS Electron microscopy Infertility Adrenal tumors Male Interstitial lung disease Genetic counselling Pneumopathie interstitielle diffuse CCDC39 Dynein arm assembly Human Diagnosis Cystic fibrosis Mutations Amylose AA SARS-CoV-2 Fièvre méditerranéenne familiale Familial mediterranean fever Inflammation Kartagener syndrome Female Insulin resistance Cilia Amyloidosis Common interstitial lung disease