A Case Report of Kartagener Syndrome
Primary Ciliary Dyskinesia (PCD) and Kartagener Syndrome (KS) are rare genetic disorders. PCD occurs in patients with recurrent sino-pulmonary infection, dextrocardia, chronic vasomotor rhinitis, and bronchiectasis. This study reports a rare case of KS for having further awareness of this disease. A...
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Veröffentlicht in: | Majallah-i dānishgāh-i ʻulūm-i pizishkī-i Qazvīn 2020-08, Vol.24 (3), p.284-293 |
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Format: | Artikel |
Sprache: | eng ; per |
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Zusammenfassung: | Primary Ciliary Dyskinesia (PCD) and Kartagener Syndrome (KS) are rare genetic disorders. PCD occurs in patients with recurrent sino-pulmonary infection, dextrocardia, chronic vasomotor rhinitis, and bronchiectasis. This study reports a rare case of KS for having further awareness of this disease. According to this study, this disease should be considered in patients with recurrent respiratory infections, because early diagnosis and timely treatment of these patients can lead to reduced irreversible complications and increased life expectancy. |
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ISSN: | 1561-3666 2423-5814 2228-7213 |
DOI: | 10.32598/JQUMS.24.3.8 |