Primary Ciliary Dyskinesia

What is PCD?

Primary Ciliary Dyskinesia (P.C.D.) is an inherited, relatively rare condition associated with an abnormality of cilia, which may affect the lungs, sinuses and ears. The mainstay of treatment is chest physiotherapy, enabling individuals to lead normal lives. Any problems resulting from P.C.D. vary from person to person. 
 
P.C.D, previously known as lmmotile Cilia syndrome, was first described in association with Kartagener's syndrome. The condition involves recurrent infections in the nose, ears, sinuses and lungs and if untreated can lead to a form of lung damage known as bronchiectasis. The clinical description of Kartagener's syndrome is bronchiectasis, sinusitis, dextrocardia (heart on the right) and situs inversus (internal organs being on the opposite side to normal). In the mid 1970's it was identified that the condition was associated with an abnormality of cilia.

Subsequently it has been realised that up to 50% of patients with P.C.D. do not have dextrocardia or situs inversus and therefore doctors may not be alerted to its presence.

 

News and Events

Article in Wellcome Trust Magazine 8/1/2010
Postponed PCD Adult Lunch from 10th January to 28th February 8/1/2010
Winter 2009 Newsletter 30/11/2009
Great South Run 24th October 2010 30/11/2009
Fiona's Colourful FM interview 1/10/2009
National Voices Survey 10/9/2009
PCD Article in Daily Express 10/9/2009
Jeans for Genes Campaign 2nd October 2009 10/9/2009
Genetic Counselling Research 8/4/2009
PCD - encouraging children to be active