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Kartagener syndrome

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Kartagener syndrome" returned 3 free, full-text review articles. First few results:
Laparoscopic sleeve gastrectomy in a patient with and Kartagener syndrome: an unusual surgical conundrum.
Last Updated: Jan 23, 2020

Kartagener syndrome is a rare autosomal recessive condition. Approximately 25% of those with suffer the syndrome. With the rising overall number and indications for bariatric surgery, this condition will be increasingly recognised. We present a case of a 25-year-old woman with and ...

[Analysis of the clinical characteristics of Kartagener syndrome in Chinese and foreign children].
Last Updated: Dec 02, 2018

To analyze the clinical characteristic of Kartagener syndrome in Chinese and foreign children.

Allergic bronchopulmonary aspergillosis in an adult with Kartagener syndrome.
Last Updated: Feb 01, 2019

Allergic bronchopulmonary aspergillosis (ABPA) is a pulmonary disorder resulting from immune responses directed against inhaled Aspergillus fumigatus antigens. It manifests with poorly controlled asthma, fleeting pulmonary opacities and structural lung damage in the form of bronchiectasis. ...

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3 Free Review Articles 7 Review Articles

Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Kartagener syndrome" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Kartagener syndrome" returned 21 free, full-text research articles. First few results:
Clinical and Genetic Analysis of Children with Kartagener Syndrome.
Last Updated: May 11, 2020

Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disorder characterized by dysfunction of motile cilia causing ineffective mucus clearance and organ laterality defects. In this study, two unrelated Portuguese children with strong PCD suspicion underwent extensive clinical ...

[Kartagener syndrome: neonatal diagnosis. A case report].
Last Updated: May 13, 2020

Kartagener Syndrome is an inherited autosomal recessive disorder characterized by primary ciliary dyskinesia and the triad of situs inversus viscerum, chronic sinus disease and bronchiectasis. Its prevalence varies from 1/15 000 to 1/30 000 but it is estimated that a lot of patients ...

[A New-born Case of Total Conus Defect and Single Coronary Artery with Situs Inversus Totalis Suspected Kartagener Syndrome].
Last Updated: Apr 03, 2019

We report a new-born case of total conus defect type ventricular septal defect (VSD) and single coronary artery with situs inversus totalis, suspected Kartagener syndrome clinically. After the birth, as the patient had suffered from respiratory distress due to high pulmonary blood ...

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21 Free Research Articles 61 Research Articles