Surgical Challenges in Papillary Thyroid Cancer Patient With Kartagener's Syndrome: A Case Report [PDF]
Clinical Case ReportsKartagener's syndrome is a rare disorder defined by situs inversus, chronic sinusitis, and bronchiectasis, with mirror‐image anatomy that may alter recurrent laryngeal nerve course and vascular structures.
Jianhao Huang +2 more
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Surgical Management of Kartagener's Syndrome With Bronchiectasis in a Pediatric Patient: A Case Report on Right Lower Lung Lobectomy in a 9‐Year‐Old Female [PDF]
Clinical Case ReportsKartagner syndrome is a rare congenital autosomal recessive disorder of ciliary movement, characterized by triad of chronic sinusitis, situs inversus and bronchiectasis leading to recurrent chest and sinuses infections.
Pakeezah Tabasum +5 more
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Management of Primary Ciliary Dyskinesia in a Kartagener's Syndrome Patient With Total Situs Inversus [PDF]
Respirology Case ReportsKartagener's syndrome is a rare, autosomal recessive disorder characterised by primary ciliary dyskinesia (PCD) resulting in impaired mucociliary clearance and situs inversus.
Ivan H. Huang +3 more
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Kartagener's Syndrome With Complications: Diagnostic Challenges in a Resource‐Limited Setting [PDF]
Clinical Case ReportsKartagener's Syndrome (KS) is a rare genetic disorder characterized by bronchiectasis, chronic sinusitis, and situs inversus. This case report presents a 14‐year‐old girl from rural Bangladesh diagnosed with KS, who exhibited progressive respiratory ...
Nahid Afsar +4 more
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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: A rare condition diagnosed in a young male patient [PDF]
Radiology Case ReportsKartagener's Syndrome is a rare autosomal recessive genetic condition, that affects the structure and function of cilia and includes a condition of situs inversus, chronic sinusitis, and bronchiectasis associated sometimes with infertility.A young ...
Marina Balbino, MD +3 more
doaj +2 more sources
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
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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Takotsubo’s Cardiomyopathy in a Patient with Kartagener’s Syndrome [PDF]
Case Reports in Medicine, 2014 A 46-year-old African-American male with past medical history significant for Kartagener’s syndrome, essential hypertension, and HIV presented with acute chest pain. ECG and troponins indicated an acute myocardial infarction.
Luis W. Dominguez +4 more
doaj +2 more sources