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Primary Ciliary Dyskinesia
Important
It is possible that the main title of the report Primary Ciliary Dyskinesiais not the name you expected.
Synonyms
- immotile cilia syndrome
- PCD
Disorder Subdivisions
- Kartagener syndrome
General Discussion
Primary ciliary dyskinesia (PCD) is an autosomal recessive genetic condition in which the microscopic cells in the respiratory system called cilia do not function normally. Ciliary dysfunction prevents the clearance of mucous from the lungs, paranasal sinuses and ears. Bacteria and other irritants in the mucous lead to frequent respiratory infections. Kartagener syndrome is a type of PCD associated with a mirror-image orientation of the internal organs (situs inversus).
Resources
American Lung Association of Connecticut
45 Ash Street
E. Hartford
CT
06108
USA
Tel: (860)289-5401
Fax: (860)289-5405
800: (800)586-4872
bcase@alact.org
http://www.alact.org
American Lung Association
61 Broadway, 6th Floor
New York
NY
10006
USA
Tel: (212)315-8700
Fax: (212)315-8870
800: (800)586-4872
http://www.lungusa.org
MUMS (Mothers United for Moral Support, Inc) National Parent-to-Parent Network
150 Custer Court
Green Bay
WI
54301-1243
USA
Tel: (920)336-5333
Fax: (920)339-0995
800: (877)336-5333
mums@netnet.net
http://www.netnet.net/mums/
PCD Foundation
4752 Park Ave
Minneapolis
MN
55407
USA
Tel: (612)822-3496
Fax: (612)822-3496
info@pcdfoundation.org
http://www.pcdfoundation.org
British Paediatric Orphan Lung Disease (BPOLD)
http://www.bpold.co.uk
For a Complete Report:
This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email orphan@rarediseases.org
Last Updated: 2/12/2008
Copyright 1988, 1989, 1996, 1999, 2007, 2008 National Organization for Rare Disorders, Inc.
WebMD Medical Reference from the National Organization of Rare Disorders
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