• 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