Evidence map›Paper›PMID 40382668›Full record

ArticleJournal of medical case reports2025

Kartagener syndrome in a young Ethiopian boy: a case report.

Habtamu Mesele Gebray, Addisu Liknaw Chekol, Samuel Addis Mihiretie, Abayneh Tunta Boye, Zeru Seyoum Wendimagegn, Zenebe Daniel Getachew

Abstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Habtamu Mesele GebrayDepartment of Internal Medicine, Woldia Comprehensive Specialized Hospital, Woldia, Ethiopia. habtamum8@gmail.com.ORCID http://orcid.org/0009-0007-1166-8566
Addisu Liknaw ChekolDepartment of Internal Medicine, Woldia Comprehensive Specialized Hospital, Woldia, Ethiopia. addisuliknaw@gmail.com.
Samuel Addis MihiretieDepartment of Internal Medicine, Woldia Comprehensive Specialized Hospital, Woldia, Ethiopia.
Abayneh Tunta BoyeSchool of Medicine, Woldia University, Woldia, Ethiopia.
Zeru Seyoum WendimagegnSchool of Medicine, Woldia University, Woldia, Ethiopia.
Zenebe Daniel GetachewSchool of Medicine, Woldia University, Woldia, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionKartagener syndrome is a subset of a larger group of ciliary motility disorders called primary ciliary dyskinesias. The syndrome includes the clinical triad of chronic sinusitis, bronchiectasis, and situs inversus. Patients usually present with recurrent respiratory tract infections due to ineffective mucociliary clearance. Females and males are equally affected. Kartagener syndrome occurs in about 1 in 32,000 to 40,000 births worldwide. CASE PRESENTATION: This case involved a 17-year-old Black African Semitic male patient who presented to our hospital with a complaint of intermittent productive cough, which started when he was 5 years old. He had a history of repeated treatment for lower respiratory tract infection and chronic sinusitis with frequent exacerbation. On examination, he had coarse crackles over the left posterior lower lung field. Heart sounds were appreciated on the right side. During imaging investigations, his chest X-ray posterior-anterior view showed dextrocardia and right side gastric shadow with left paracardiac bronchiectatic changes. A high-resolution chest computed tomography scan was suggestive of complete situs inversus. There were left lower lobe bronchiectatic changes. An electrocardiogram showed features of dextrocardia. Routine laboratory tests were within normal range. He was treated with thoracic physiotherapy, azithromycin 500 mg three times per week, and mucolytics, with no apparent exacerbations in the last 6 months.

conclusionThe diagnosis of Kartagener syndrome is typically delayed because the clinical symptoms are easily mistaken for common infections. Since there is no specific treatment for Kartagener syndrome, early diagnosis and management of Kartagener syndrome are critical to prevent irreversible lung damage and chronic lifelong sequelae. A high index of suspicion is needed to make an early diagnosis so that timely treatment options may be offered to prevent problems associated with Kartagener syndrome.

Indexed as

Kartagener SyndromeAdolescentAnti-Bacterial AgentsAzithromycinBronchiectasisCoughDextrocardiaElectrocardiographyEthiopiaHumansMalePhysical Therapy ModalitiesSitus InversusTomography, X-Ray ComputedTreatment OutcomeAnti-Bacterial AgentsAzithromycinBronchiectasisDextrocardiaKartagener syndromePrimary ciliary dyskinesiasSitus inversus

Identifiers

PMID40382668
PMCPMC12085034

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.