AI Article Synopsis
- - Kartagener syndrome is a rare genetic disorder that can cause ongoing respiratory issues and specific changes in imaging, like bronchiectasis and situs inversus.
- - Adults with this condition often experience persistent respiratory symptoms that should raise clinical suspicion among healthcare providers.
- - Early diagnosis and proper treatment are essential to help protect lung function and improve quality of life for those affected.
Article Abstract
Kartagener syndrome, a rare genetic disorder, can present in adults with persistent respiratory symptoms and radiological changes, such as bronchiectasis and situs inversus. Clinicians should maintain a high clinical suspicion, as early recognition and appropriate management are crucial for preserving pulmonary function.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10880418 | PMC |
| http://dx.doi.org/10.1002/rcr2.1309 | DOI Listing |
Publication Analysis
Top Keywords
situs inversus
8
persistent cough
4
cough situs
4
inversus middle-aged
4
middle-aged female
4
female kartagener
4
kartagener syndrome
4
syndrome rare
4
rare genetic
4
genetic disorder
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!