Primary ciliary dyskinesia (PCD) is a rare disorder that involves abnormal cilia. These are microscopic, hairlike structures that line your lungs and other areas. Here, they help move germs, waste and dust. …

Join the inaugural Global PCD Conference in Montreal, Canada—an international event dedicated to the science and clinical care of primary ciliary dyskinesia.

Jul 12, 2022 · Primary ciliary dyskinesia, or PCD, is a rare genetic condition that affects the body’s ability to remove mucus. This leads to frequent infections in the sinuses, ears, and lungs. Learn more about …

Diagnosing primary ciliary dyskinesia (PCD) has traditionally been challenging, often relying on detailed analysis of ciliary structure through tissue biopsies. The Diagnostic Process Getting a PCD diagnosis …

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 and adults.

Jan 21, 2026 · Primary Ciliary Dyskinesia Symptoms and Diagnosis What Are the Symptoms of PCD? The symptoms and severity of PCD vary from person to person, and over time. Typically, the first …

Get the facts about the rare inherited disorder primary ciliary dyskinesia (PCD), including how it's diagnosed and treated at The Children's Hospital of Philadelphia. What is Primary Ciliary …

Primary ciliary dyskinesia (PCD) is a progressive disorder, meaning it can worsen over time. Fortunately, for most people, the progression is slow. We encourage patients and caregivers to review the […]

What is Primary Ciliary Dyskinesia (PCD)? PCD is a rare, inherited (genetic) condition that affects tiny, hair-like structures called cilia. These cilia line many parts of the body, including the nose, sinuses, …

Amphenol PCD designs and manufactures circular and rectangular electronic connectors for low, medium and high power applications and lightweight composite cable and pipe management …