hereditary otorhinolaryngologic disease familial nasal acilia https://rarediseases.info.nih.gov/diseases/2254/familial-nasal-acilia https://www.malacards.org/card/familial_nasal_acilia GARD:0002254 SCTID:763532008 UMLS:C4706505 MONDO:0019634 MEDGEN:1647725 Orphanet:922 Familial nasal acilia is a rare genetic otorhinolaryngologic disease characterized by respiratory morbidity due to lack of cilia on the respiratory tract epithelial cells. The disease manifests from birth with respiratory distress, neonatal pneumonia, dyspnea, lobar atelectasis and bronchiectasis. Recurrent infections of the upper and lower respiratory tract, chronic humid coughing, and chronic sinusitis, otitis and rhinitis are typical lifelong presenting conditions.