z-logo
open-access-imgOpen Access
Kartagener′s syndrome: A case series
Author(s) -
Mayank Mishra,
Naresh Kumar,
Ashish Jaiswal,
Ajay Kumar Verma,
Surya Kant
Publication year - 2012
Publication title -
lung india
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 25
eISSN - 0974-598X
pISSN - 0970-2113
DOI - 10.4103/0970-2113.102831
Subject(s) - medicine , series (stratigraphy) , kartagener syndrome , primary ciliary dyskinesia , bronchiectasis , lung , biology , paleontology
Kartagener's syndrome is a rare, autosomal recessive genetic ciliary disorder comprising the triad of situs inversus, chronic sinusitis, and bronchiectasis. The basic problem lies in the defective movement of cilia, leading to recurrent chest infections, ear/nose/throat symptoms, and infertility. We hereby report three unusual cases of this rare entity - an infertile male with azoospermia in whom Bochdalek's diaphragmatic hernia coexisted, another case of an infertile female, and a third of an infertile male with oligospermia. The need for a high index of suspicion to make an early diagnosis cannot be overemphasized in such patients so that wherever possible, options for timely treatment of infertility may be offered and unnecessary evaluation of symptoms is avoided.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here