Biallelic Variants in CCDC39 Gene Lead to Primary Ciliary Dyskinesia and Kartagener Syndrome. [PDF]
Biomed Res Int, 2022 Shi X +6 more
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The EZ-Blocker® for one-lung ventilation in a patient with Kartagener syndrome and tracheal bronchus -a case report. [PDF]
Korean J Anesthesiol, 2023 Hwang BY +6 more
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Liver Transplantation in a Child with Kartagener Syndrome: A Case Report. [PDF]
Int Med Case Rep J, 2021 Uludag Yanaral T +4 more
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Case Report: Rare Dynein Axonemal Heavy Chain 9 Mutations in a Han-Chinese Patient With Kartagener Syndrome. [PDF]
Front Med (Lausanne), 2022 Feng J +5 more
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Unraveling the Puzzle: A Case Report on Kartagener Syndrome with Young's Syndrome
<p>Primary ciliary dyskinesia is an autosomal recessive disorder associated with abnormal ciliary structure and function, which results in retention of mucus and bacteria in respiratory tract, leading to chronic oto-sino-pulmonary disease, situs ...
Megha K. Airao +5 more
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Morphological Adaptation after Bilateral Lung Transplantation in a Patient with Kartagener Syndrome: A Case Report. [PDF]
J Chest Surg, 2022 Kim CH, Son BS, Son J, Kim DH.
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Laparoscopic Sleeve Gastrectomy in a Patient With Situs Inversus Totalis and Kartagener Syndrome. [PDF]
Cureus, 2021 Almussallam B +8 more
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, 2019 Kartagener syndrome is an autosomic recessive hereditary disease characterized of primary ciliary dyskinesia, chro- nic cough, chronic sinusitis, infertility, situs inversus, and bronchiectasis.
Orozco, Karen Luna +3 more
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Clinical features, misdiagnosis, and treatment of clinically diagnosed complete Kartagener syndrome: A three-case series for primary care. [PDF]
SAGE Open Med Case RepLi D, Wang Z.
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