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