A Case Report of Kartagener Syndrome

M. Moradi, L. Yekefallah, M. Zohal, P. Namdar
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引用次数: 0

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.
Kartagener综合征1例报告
原发性纤毛运动障碍(PCD)和Kartagener综合征(KS)是罕见的遗传性疾病。PCD常见于复发性肺感染、右心、慢性血管舒缩性鼻炎和支气管扩张的患者。本研究报告了一例罕见的KS病例,对这种疾病有进一步的认识。根据本研究,复发性呼吸道感染患者应考虑此病,因为这些患者的早期诊断和及时治疗可减少不可逆转的并发症,延长预期寿命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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7
审稿时长
4 weeks
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