A Case Report of Kartagener Syndrome

Authors

mahnaz moradi1, leili yekefallahleili yekefallah ORCID1, mohammad ali zohal2, Peyman Namdar3,*
1Department of Critcal Care Nursing, School of Nursing and Midwifery, Qazvin University of Medical Sciences, Qazvin, Iran.
2Department of Internal Medicine, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
3Department of Surgery, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
*Corresponding Author: Department of Surgery, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran. Email: [email protected]

Journal of Inflammatory Diseases:Vol. 24, issue 3; 284-293
Published online:Sep 30, 2020
Article type:Case Report
How to Cite:moradi M, yekefallah L, zohal MA, Namdar P. A Case Report of Kartagener Syndrome. J Inflamm Dis. 2024;24(3):e156223. doi:

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.

Copyright

© 2024, Journal of Inflammatory Diseases. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.

Similar Articles

8
Oct
2023
Analysis of Clinical Characteristics and Gene Variants Associated with Primary Ciliary Dyskinesia

Analysis of Clinical Characteristics and Gene Variants Associated with Primary Ciliary Dyskinesia

Qionghua Chen,
Jingyang Zheng,
lie Zeng,
Liduan Su,
Chunyan Lin,
Dongyi Pan

Chen Q, Zheng J, Zeng L, Su L, Lin C, et al. Analysis of Clinical Characteristics and Gene Variants Associated with Primary Ciliary Dyskinesia. Inn J Pediatr. 2023;33(5):e132964. doi: https://doi.org/10.5812/ijp-132964

6
Jan
2021

Investigation of Primary Ciliary Dyskinesia in Children with Bronchiectasis in Iran

Sohila Alyasin,
Behjat Maneshian,
Shadi Niliyeh

Alyasin S, Maneshian B, Niliyeh S. Investigation of Primary Ciliary Dyskinesia in Children with Bronchiectasis in Iran. Shiraz E-Med J. 2021;22(6):e104562. doi: https://doi.org/10.5812/semj.104562

30
Jun
2017

Sydenham Chorea in a Girl with Dextrocardia and Situs Inversus

alireza vakilian,
Reza Derakhshan Ravari,
Amir Moghadam-Ahmadi

vakilian A, Derakhshan Ravari R, Moghadam-Ahmadi A. Sydenham Chorea in a Girl with Dextrocardia and Situs Inversus. Int Cardiovasc Res J. 2017;11(2):e11188. doi:

29
May
2013

Holoprosencephaly and Klinefelter Syndrome

Mehrnoosh Mousaviagdas,
Shahin Abdollahifakhim,
Ebrahim Sakhinia

Mousaviagdas M, Abdollahifakhim S, Sakhinia E. Holoprosencephaly and Klinefelter Syndrome. Inn J Pediatr. 2014;24(2):. doi:

31
Jul
2017
Shone’s Syndrome and Patent Ductus Arteriosus: A Rare Case Report

Shone’s Syndrome and Patent Ductus Arteriosus: A Rare Case Report

Zahra Khajali,
Marziyeh Pakbaz,
Alireza Alizadeh Ghavidel,
Azin Alizadehasl

Khajali Z, Pakbaz M, Alizadeh Ghavidel A, Alizadehasl A. Shone’s Syndrome and Patent Ductus Arteriosus: A Rare Case Report. Multidiscip Cardio Annal. 2018;9(1):e58875. doi: https://doi.org/10.5812/mcardia.58875

More by these authors

mahnaz moradiPubMedScholar
leili yekefallahPubMedScholar
mohammad ali zohalPubMedScholar
Peyman NamdarPubMedScholar
Share
Cited by
Metrics