Primary ciliary dyskinesia (PCD) is a rare genetic disease leading to bronchiectasis in most patients. In addition to the lungs, PCD might affect multiple organ systems, and patients frequently have multiple clinical problems, which require multidisciplinary management. Diagnosis of PCD needs a combination of tests, many of which require expertise and expensive equipment. Measurement of nasal nitric oxide is the first test to consider when PCD is suspected. Detailed clinical history using available predictive scores in combination with information on functional and structural aspects of lung disease is important to identify which patients should be referred for further diagnostic testing.</p
Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sinopulmona...
The diagnosis of primary ciliary dyskinesia (PCD) has relied on analysis of ciliary motility and ult...
Bronchiectasis represents the final pathway of several infectious, genetic, immunologic or allergic ...
Primary ciliary dyskinesia (PCD) is a rare genetic disease leading to bronchiectasis in most patient...
Primary ciliary dyskinesia (PCD) is a rare genetic disease leading to bronchiectasis in most patient...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is a recessive genetically heterogeneous disorder of motile cilia w...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary Ciliary Dyskinesia (PCD) is a rare, under-recognized disease that affects respiratory ciliar...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure, function, an...
Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive, and in classical fo...
Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sinopulmona...
The diagnosis of primary ciliary dyskinesia (PCD) has relied on analysis of ciliary motility and ult...
Bronchiectasis represents the final pathway of several infectious, genetic, immunologic or allergic ...
Primary ciliary dyskinesia (PCD) is a rare genetic disease leading to bronchiectasis in most patient...
Primary ciliary dyskinesia (PCD) is a rare genetic disease leading to bronchiectasis in most patient...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is a recessive genetically heterogeneous disorder of motile cilia w...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary Ciliary Dyskinesia (PCD) is a rare, under-recognized disease that affects respiratory ciliar...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure, function, an...
Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive, and in classical fo...
Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sinopulmona...
The diagnosis of primary ciliary dyskinesia (PCD) has relied on analysis of ciliary motility and ult...
Bronchiectasis represents the final pathway of several infectious, genetic, immunologic or allergic ...