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"KARTAGENER SYNDROME"

“ This is a type of primary ciliary dyskinesia with autosomal recessive inheritance . It comprises a triad of dextrocardia, bronchiectasis ...

This is a type of primary ciliary dyskinesia with autosomal recessive inheritance. It comprises a triad of dextrocardia, bronchiectasis and sinusitis. The problem is due to ciliary dysfunction; in the lungs, this leads to bronchitis, recurrent pneumonia, etc. It usually presents in childhood and is associated with infertility, corneal abnormalities, transposition of the great vessels, pyloric stenosis, post-cricoid web and epispadias.
PLAIN FILM
•  Classic findings are bronchiectasis and dextrocardia.
•  Check also for bronchial wall thickening, collapse and consolidation.