Primary ciliary dyskinesia (PCD)

Primary ciliary dyskinesia (PCD) is a rare inherited condition. Our information explains what PCD is, the signs and symptoms, how PCD is diagnosed, and how it’s treated.

Asthma + Lung UK

What is primary ciliary dyskinesia (PCD)?

Primary ciliary dyskinesia (PCD) is a rare, inherited, long-term condition that children are born with.
Asthma + Lung UK

What is the treatment for PCD?

The aim of treatment for primary ciliary dyskinesia (PCD) is to improve or maintain your child’s normal lung function. On this page, we explain the treatments available, including antibiotics, inhaled medication and daily airway clearance.
Asthma + Lung UK

How is PCD diagnosed?

Did you find this information useful?

We use your comments to improve our information. We cannot reply to comments left on this form. If you have health concerns or need clinical advice, call our helpline on 0300 222 5800 between 9am and 5pm on a weekday or email them.

Page last reviewed:
Next review due: