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
Wrongly Diagnosed with Kartagener syndrome?
Kartagener syndrome: Related Patient Stories
Kartagener syndrome: Deaths
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Kartagener syndrome: Complications
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Causes of Kartagener syndrome
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Disease Topics Related To Kartagener syndrome
Research the causes of these diseases that are similar to, or related to, Kartagener syndrome:
Kartagener syndrome: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Hospitals & Clinics: Kartagener syndrome
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on hospital performance and surgical care quality:
Kartagener syndrome: Rare Types
Rare types of diseases and disorders in related medical categories:
Evidence Based Medicine Research for Kartagener syndrome
Medical research articles related to Kartagener syndrome include:
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Research about Kartagener syndrome
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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
Statistics for Kartagener syndrome
Kartagener syndrome: Broader Related Topics
Types of Kartagener syndrome
User Interactive Forums
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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
Contents for Kartagener syndrome: