Kartagener syndrome – the complexity of a primary ciliary dyskinesia phenotype and its rare association with cystic fibrosis: case report Cover

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Kartagener syndrome – the complexity of a primary ciliary dyskinesia phenotype and its rare association with cystic fibrosis: case report

Volume 74 (2025): Issue 1 (January 2025)

By: Roxana-Ștefania Cobzariu, Cristian Cojocaru and Radu Crișan-Dabija

Open Access

|Jan 2026

Authors

Roxana-Ștefania Cobzariu

cobzariuroxana6@gmail.com

Pneumology Department, Clinical Hospital of Pulmonary Diseases, Iasi, Romania

Cristian Cojocaru

Pneumology Department, Clinical Hospital of Pulmonary Diseases, Iasi, Romania

Pneumology Department, Faculty of General Medicine, Grigore T. Popa University of Medicine and Pharmacy, Iasi, Romania

Radu Crișan-Dabija

Pneumology Department, Clinical Hospital of Pulmonary Diseases, Iasi, Romania

Pneumology Department, Faculty of General Medicine, Grigore T. Popa University of Medicine and Pharmacy, Iasi, Romania

DOI: https://doi.org/10.2478/pneum-2025-0036 | Journal eISSN: 2247-059X | Journal ISSN: 2067-2993

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Language: English

Page range: 125 - 130

Published on: Jan 14, 2026

Published by: Romanian Society of Pneumology

In partnership with: Paradigm Publishing Services

Publication frequency: Volume open

Keywords:

primary ciliary dyskinesia,

Kartagener syndrome,

cystic fibrosis,

Related subjects:

Clinical medicine,

Clinical medicine, other,

Internal medicine,

© 2026 Roxana-Ștefania Cobzariu, Cristian Cojocaru, Radu Crișan-Dabija, published by Romanian Society of Pneumology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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