Moradi, Mahnaz and Yekefallah, Leili and Zohal, Mohammadali and Namdar, Peyman (2020) A Case Report of Kartagener Syndrome. The Journal of Qazvin University of Medical Sciences, 24 (3). pp. 284-293. ISSN 24235814
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Abstract
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.
Item Type: | Article |
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Subjects: | R Medicine > RT Nursing |
Divisions: | University Portal > vice chancellor > vcr |
Depositing User: | pr vcen research |
Date Deposited: | 08 Feb 2021 10:44 |
Last Modified: | 08 Feb 2021 10:44 |
URI: | http://eprints.qums.ac.ir/id/eprint/10507 |
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