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Diagnosis of Primary Ciliary Dyskinesia

Myrofora Goutaki, Amelia Shoemark

2022Clinics in Chest Medicine77 citationsDOIOpen Access PDF

Abstract

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.

Topics & Concepts

Primary ciliary dyskinesiaMedicineBronchiectasisIntensive care medicineDiseaseDiagnostic testGenetic testingPathologyLungPediatricsInternal medicineCystic Fibrosis Research AdvancesNeonatal Respiratory Health ResearchTracheal and airway disorders
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