Primary ciliary dyskinesia (PCD) is a rare genetic condition that can lead to chronic lung, ear and sinus infections, along with other disorders in children ...
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Nov 24, 2011 · Background. Primary ciliary dyskinesia (PCD) is a rare genetically induced disorder of cilia inducing mainly respiratory diseases.
Primary ciliary dyskinesia (PCD) is a rare inherited disorder caused by defects in the structure and/or function of cilia. Cilia are tiny hair ...
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Mayo Clinic Laboratories' PCD test offerings include both electron microscopy evaluation (EM) and genetic testing. Highly trained, board-certified pathologists ...
Primary ciliary dysfunction (PCD), first described in 1976, is a disorder of the structure and function of motile cilia that results in chronic ...
Missing: Pathology | Show results with:Pathology
Feb 4, 2022 · Primary ciliary dyskinesia (PCD) is a rare, inherited disorder. It affects cilia, tiny hair-like organs that help your body clear mucus.
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Jan 29, 2024 · INTRODUCTION. Primary ciliary dyskinesia (PCD, also called the immotile-cilia syndrome) is characterized by congenital impairment of ...
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia characterised by chronic lung disease, rhinosinusitis, hearing ...
PCD is caused by a defect in cilia, which are microscopic, hair-like structures on the surface of the cells of the respiratory tract. Cilia are responsible for ...
Missing: Pathology | Show results with:Pathology
Primary ciliary dyskinesia (PCD) is a disorder of ciliary function and structure that is associated clinically with male infertility, otosinopulmonary disease, ...
