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 ...
People also ask
What is PCD in pathology?
What is the pathophysiology of PCD?
What does PCD mean in medical terms?
What is the difference between Kartagener and PCD?
Nov 24, 2011 · Background. Primary ciliary dyskinesia (PCD) is a rare genetically induced disorder of cilia inducing mainly respiratory diseases.
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
Mayo Clinic Laboratories' PCD test offerings include both electron microscopy evaluation (EM) and genetic testing. Highly trained, board-certified pathologists ...
Primary ciliary dyskinesia (PCD) is a rare inherited disorder caused by defects in the structure and/or function of cilia. Cilia are tiny hair ...
Missing: Pathology | Show results with:Pathology
Primary ciliary dyskinesia (PCD) is a rare, inherited disorder. It affects cilia, tiny hair-like organs that help your body clear mucus.
Missing: Pathology | Show results with:Pathology
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, ...
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia characterised by chronic lung disease, rhinosinusitis, hearing ...
Summary Primary ciliary dyskinesia (PCD) is a rare heterogeneous genetic disorder affecting ciliary function. Genes coding for various ciliary structural ...