Kartagener’s syndrome: A case report
Introduction. Kartagener’s syndrome is a recessive autosomal disease which is mainly seen to affect ciliary movement. The symptoms of the syndrome are the consequence of the defective motility of the cilia found in the respiratory tract and that results with recurrent lung infections caused by mucus...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Military Health Department, Ministry of Defance, Serbia
2016-01-01
|
Series: | Vojnosanitetski Pregled |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0042-8450/2016/0042-84501600072T.pdf |
id |
doaj-f26b7a7941d94e9eb8c726bd33574571 |
---|---|
record_format |
Article |
spelling |
doaj-f26b7a7941d94e9eb8c726bd335745712020-11-25T00:28:57ZengMilitary Health Department, Ministry of Defance, SerbiaVojnosanitetski Pregled0042-84502406-07202016-01-0173987387610.2298/VSP141020072T0042-84501600072TKartagener’s syndrome: A case reportTaušan Đorđe0Ristić Anđelka1Zvezdin Biljana2Military Medical Academy, Clinic for Lung Diseases, BelgradeMilitary Medical Academy, Clinic for Emergency and Internal Medicine, Belgrade + University of Defence, Faculty of Medicine of the Military Medical Academy, BelgradeInstitute for Pulmonary Diseases of Vojvodina, Sremska Kamenica + Faculty of Medicine, Novi SadIntroduction. Kartagener’s syndrome is a recessive autosomal disease which is mainly seen to affect ciliary movement. The symptoms of the syndrome are the consequence of the defective motility of the cilia found in the respiratory tract and that results with recurrent lung infections caused by mucus stasis in the bronchi. Case report. A 37-year-old married, male father of one child, presented with a history of productive cough, wheezing, dispnea, headache, temporary fever. In his 9th year of age, 1986, situs inversus, sinusitis and pectus excavatum were diagnosed. In 1994 he was operated for correction of pectus excavatum. Bronchial asthma was diagnosed in 2008 when he was 31. In the last 2 years he had episodes of breathlessness, wheezing, cough, expectoration, headache, fever and fast declining lung function. The patient was treated with combination of inhaled bronchodilatators (inhaled corticosteroids + long-acting β-2 agonist), and occasional administration of antibiotics, oral prednisolone, mucolytics in episodes of exacerbations of disease over a period of 7−14 days. Conclusion. Treatment for patients with this syndrome has not been established yet, but it is important to control chronic lung infections and prevent declining of lung function.http://www.doiserbia.nb.rs/img/doi/0042-8450/2016/0042-84501600072T.pdfKartagener syndromerespiratory tract infectionbronhiectasistherapeuticsfertility |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Taušan Đorđe Ristić Anđelka Zvezdin Biljana |
spellingShingle |
Taušan Đorđe Ristić Anđelka Zvezdin Biljana Kartagener’s syndrome: A case report Vojnosanitetski Pregled Kartagener syndrome respiratory tract infection bronhiectasis therapeutics fertility |
author_facet |
Taušan Đorđe Ristić Anđelka Zvezdin Biljana |
author_sort |
Taušan Đorđe |
title |
Kartagener’s syndrome: A case report |
title_short |
Kartagener’s syndrome: A case report |
title_full |
Kartagener’s syndrome: A case report |
title_fullStr |
Kartagener’s syndrome: A case report |
title_full_unstemmed |
Kartagener’s syndrome: A case report |
title_sort |
kartagener’s syndrome: a case report |
publisher |
Military Health Department, Ministry of Defance, Serbia |
series |
Vojnosanitetski Pregled |
issn |
0042-8450 2406-0720 |
publishDate |
2016-01-01 |
description |
Introduction. Kartagener’s syndrome is a recessive autosomal disease which is mainly seen to affect ciliary movement. The symptoms of the syndrome are the consequence of the defective motility of the cilia found in the respiratory tract and that results with recurrent lung infections caused by mucus stasis in the bronchi. Case report. A 37-year-old married, male father of one child, presented with a history of productive cough, wheezing, dispnea, headache, temporary fever. In his 9th year of age, 1986, situs inversus, sinusitis and pectus excavatum were diagnosed. In 1994 he was operated for correction of pectus excavatum. Bronchial asthma was diagnosed in 2008 when he was 31. In the last 2 years he had episodes of breathlessness, wheezing, cough, expectoration, headache, fever and fast declining lung function. The patient was treated with combination of inhaled bronchodilatators (inhaled corticosteroids + long-acting β-2 agonist), and occasional administration of antibiotics, oral prednisolone, mucolytics in episodes of exacerbations of disease over a period of 7−14 days. Conclusion. Treatment for patients with this syndrome has not been established yet, but it is important to control chronic lung infections and prevent declining of lung function. |
topic |
Kartagener syndrome respiratory tract infection bronhiectasis therapeutics fertility |
url |
http://www.doiserbia.nb.rs/img/doi/0042-8450/2016/0042-84501600072T.pdf |
work_keys_str_mv |
AT tausanđorđe kartagenerssyndromeacasereport AT risticanđelka kartagenerssyndromeacasereport AT zvezdinbiljana kartagenerssyndromeacasereport |
_version_ |
1725333574832357376 |