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Kartagener syndrome



Kartagener syndrome: Introduction

Kartagener syndrome: A rare genetic disorder characterized by enlarged bronchial tubes, sinusitis and cross-positioning of body organs. More detailed information about the symptoms, causes, and treatments of Kartagener syndrome is available below.

Symptoms of Kartagener syndrome

See full list of 18 symptoms of Kartagener syndrome

Kartagener syndrome: Complications

Review possible medical complications related to Kartagener syndrome:

Medical Textbooks Online about Kartagener syndrome

Medical Books Excerpts
  • "Professional Guide to Diseases (Eighth Edition)" (2005)
  • "Professional Guide to Signs & Symptoms (Fifth Edition)" (2006)
  • "Handbook of Diseases" (2003)

Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Wrongly Diagnosed with Kartagener syndrome?

Causes of Kartagener syndrome

Read more about causes of Kartagener syndrome.

Evidence Based Medicine Research for Kartagener syndrome

Medical research articles related to Kartagener syndrome include:

Click here to find more evidence-based articles on the TRIP Database

Videos for Kartagener syndrome

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Reseach about Kartagener syndrome

Visit our research pages for current research about Kartagener syndrome treatments.

Clinical Trials for Kartagener syndrome

The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on ClinicalTrials.gov for Kartagener syndrome include:

Read more about Clinical Trials for Kartagener syndrome

Stories from Users Related to Kartagener syndrome

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Definitions of Kartagener syndrome:

An autosomal recessive disorder characterized by BRONCHIECTASIS; SINUSITIS; DEXTROCARDIA; and INFERTILITY. In vitro studies of tissues from these patients, have shown various patterns of abnormal ciliary beating. (Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/OMIM, MIM # 244400, April 24, 2001) - (Source - Diseases Database)

Kartagener syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Kartagener syndrome, or a subtype of Kartagener syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Kartagener syndrome as a "rare disease".
Source - Orphanet


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