Article
[Primary ciliary dyskinesia].
Innere Medizin (Heidelberg, Germany) - 1 Jun 2024
Raidt Johanna, Staar Ben O, Omran Heymut, Ringshausen Felix C
Abstract excerpt
Primary ciliary dyskinesia (PCD) is a rare genetic disorder with a variable clinical phenotype that is accompanied by reduced motility of the cilia in the respiratory tract and numerous other organs. This leads to various characteristic symptoms and disease manifestations, primarily affecting the lungs (chronic persistent productive cough, bronchiectasis), the nose and paranasal sinuses (chronic persistent...
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