A Case Report of Kartagener Syndrome
| Author | mahnaz moradi | en |
| Author | leili yekefallah | en |
| Author | mohammad ali zohal | en |
| Author | Peyman Namdar | en |
| Orcid | leili yekefallah [0000-0001-7425-9451] | en |
| Issued Date | 2020-09-30 | en |
| 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. | en |
| DOI | https://doi.org/ | en |
| Keyword | Primary ciliary dyskinesia | en |
| Keyword | Kartagener syndrome | en |
| Keyword | Dextrocardia | en |
| Keyword | Situs inversus | en |
| Publisher | Brieflands | en |
| Title | A Case Report of Kartagener Syndrome | en |
| Type | Case Report | en |