Take your place in the future of PCD
Take your place in the future of PCD
It’s estimated that around one in 10,000
people has PCD, with approximately
46,000 undiagnosed in the US.
PCD is a rare genetic disorder that affects the cilia, the tiny hair-like structures on the surface of cells that line the upper and lower airways. Symptoms of PCD are:
A persistent cough
Recurrent ear infections
Family history of PCD
And more...
L E A R N M O R E
Thank you
Thank you for your interest in Primary Ciliary Dyskinesia (PCD) research, this study has now closed for enrollment. To follow the research progress and outcomes of clinical trials in PCD, you can follow the link below.