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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

Wrongly Diagnosed with Kartagener syndrome?

Kartagener syndrome: Related Patient Stories

Kartagener syndrome: Deaths

Read more about Deaths and Kartagener syndrome.

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

Research quality ratings and patient safety measures for medical facilities in specialties related to Kartagener syndrome:

Choosing the Best Hospital: More general information, not necessarily in relation to Kartagener syndrome, 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:

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

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:

Statistics for Kartagener syndrome

Kartagener syndrome: Broader Related Topics

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

 

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