{"id":12531,"date":"2024-10-11T20:00:03","date_gmt":"2024-10-11T18:00:03","guid":{"rendered":"https:\/\/valintermed.com\/?p=12531"},"modified":"2024-10-11T20:00:03","modified_gmt":"2024-10-11T18:00:03","slug":"pervichnaya-tsiliarnaya-diskineziya-ptsd","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/primary-ciliars-diskinezia-ptsd\/","title":{"rendered":"Primary ciliary dyskinesia (PCD)"},"content":{"rendered":"
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Primary ciliary dyskinesia (PCD) is a genetic disorder characterized by dysfunction of the cilia, resulting in decreased mucociliary clearance. Cilia are microscopic structures on the surface of cells in the respiratory tract that are essential for removing mucus and particles from the respiratory tract. In PCD, the normal movement of the cilia is lost, leading to mucus accumulation, frequent respiratory infections, and may also cause bronchiectasis. The disorder is caused by defects in the structure or function of the cilia, usually due to mutations in a number of genes that control their formation and function. PCD is a rare condition, but its public health and diagnostic importance should not be underestimated, as it requires a comprehensive approach to treatment and monitoring.<\/p>\n

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