Author/Authors
NURAL, Serkan Afyon Kocatepe Üniversitesi - Tıp Fakültesi - Göğüs Hastalıkları AD, Turkey , HALICI, Bilal Afyon Kocatepe Üniversitesi - Tıp Fakültesi - Göğüs Hastalıkları AD, Turkey , GÜNAY, Ersin Afyon Kocatepe Üniversitesi - Tıp Fakültesi - Göğüs Hastalıkları AD, Turkey
Title Of Article
A Rare Case of Kartagener’s Syndrome with Delayed Diagnosis
شماره ركورد
42142
Abstract
Kartagener’s syndrome is an autosomal recessive inherited, primary ciliary dyskinesia syndrome, which is characterized by situs inversus, bronchiectasis, and chronic sinusitis. Symptoms usually emerge during childhood period. Ninety percent of cases are diagnosed prior to 15 years of age. In patients with Kartagener’s syndrome, respiratory infections are encountered such as chronic coughing, mucoid sputum, and recurrent pneumonia attacks. Bronchiectasis develops as a result of recurrent lung infections. We presented a fifteen year old male patient who had a history of recurrent respiratory infections has been diagnosed with Kartagener’s syndrome with the guidance of literature survey.
From Page
191
NaturalLanguageKeyword
Kartagener’s syndrome , situs inversus , bronchiectasis
JournalTitle
Kocatepe Medical Journal
To Page
193
JournalTitle
Kocatepe Medical Journal
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