Spot the Signs of Primary Ciliary Dyskinesia (PCD)

Participants will learn to identify key cardinal signs that may indicate PCD in children, particularly those with persistent nasal congestion, chronic wet cough, recurrent respiratory infections, and neonatal respiratory distress. Recognizing these symptoms early is crucial for timely intervention. Since PCD diagnosis is complex and lacks a single definitive test, the session explores strategies for navigating patients through the diagnostic process, including nasal nitric oxide testing, genetic analysis, and high-resolution microscopy of ciliary function. Clinicians will gain insights into optimizing referral pathways and confirming the condition. Additionally, the webinar highlights the multidisciplinary approach to PCD management, emphasizing collaboration among pulmonologists, ENT specialists, physiotherapists, and genetic counselors. A structured care framework ensures better symptom control, improved respiratory health, and long-term patient support.