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Pulmonary Hypertension in a Patient With Kartagener’s Syndrome and a Novel Homozygous Nonsense Mutation in CCDC40 Gene: A Case Report [PDF]
Frontiers in Medicine, 2022 Kartagener’s syndrome is a subgroup of primary ciliary dyskinesia (PCD), a genetically heterogeneous condition characterised by sinusitis, bronchiectasis, and situs in versus. Genetic testing has importance for their diagnosis.
Hai-Long Dai +3 more
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Kartagener’s syndrome: a case report [PDF]
Journal of Medical Case Reports, 2018 Background Kartagener’s syndrome is a subset of primary ciliary dyskinesia, an autosomal recessive inherited disorder characterized by the clinical triad of chronic sinusitis, bronchiectasis, and situs inversus.
Abilo Tadesse +3 more
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Kartagener’s Syndrome Complicated by Bronchiectasis with Tricuspid and Mitral Valve Regurgitation: A Case Report [PDF]
Clinical Medicine Insights: Case ReportsBackground: Kartagener’s syndrome, a rare autosomal recessive genetic disorder, is characterized by primary ciliary dyskinesia (PCD), resulting in defective cilia function in the respiratory tract and fallopian tubes.
Rayyan Vaid +2 more
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Kartagener's syndrome: A case report [PDF]
Journal of Krishna Institute of Medical Sciences University, 2023 The primary defect in Kartagener's syndrome is at the ciliary level and so the normal ciliary activity is compromised causing impaired respiratory tract clearance, infertility and defective organ(s) orientation and left-right laterality predisposition ...
B. Shashidhar Reddy +2 more
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The Pan African Medical Journal, 2018 A 29-year-old non-smoker male with a history of chronic cough, and recurrent pneumonia, sinusitis and otomastoiditis was admitted to the emergency room with a 3-day history of headache, cough productive and dyspnea.
Rodolfo Mendes Queiroz +1 more
doaj +2 more sources
Association of bronchectasies and situs inversus
Egyptian Journal of Chest Disease and Tuberculosis, 2014 Kartagener’s syndrome comprises a rare clinical triad: nasal polyposis, bronchiectasis and situs inversus. It is a hereditary disease transmitted as an autosomal recessive trait, characterized by a partial or total failure of the eyelashes vibration ...
H. Kouismi +3 more
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Kartagener syndrome with partial anomalous pulmonary venous drainage: a case report [PDF]
Journal of Medical Case ReportsBackground Kartagener syndrome, defined by situs inversus, bronchiectasis, and chronic sinusitis. This condition rarely coexists with cardiac anomalies.
Dwika Rasyid Firmanda +6 more
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A rare case of kartagener's syndrome with schizophrenia
Annals of Indian Psychiatry, 2022 Kartagener's syndrome is a rare genetic disorder of primary ciliary dyskinesia characterized by the triad of bronchiectasis, sinusitis, and situs inversus. There is limited data on the role of Kartagener's syndrome leading to psychotic manifestations. We
Prerna Balkrishen Khar +3 more
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A new phenotype of Kartagener's syndrome: An interesting case report
Indian Journal of Ophthalmology. Case Reports, 2021 Kartagener's syndrome (KS) is Primary Ciliary Dyskinesia, autosomal recessive disorder characterised by triad of situs inversus of viscera, sinusitis, bronchiectasis due to ciliary dysfunction.
Kalpana Badami Nagaraj +5 more
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Kartagener’s Syndrome: A Narrative Review on its Clinical Implications and Management [PDF]
Journal of Clinical and Diagnostic ResearchKartagener’s Syndrome, alternatively known as Primary Ciliary Dyskinesia (PCD) is a rare and intricate inherited disorder that impacts the structure and function of cilia, leading to compromised mucociliary clearance.
Samanvita Kaza, Darshna G Fulmali
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