Rheumatoid Arthritis, Kartagener’s Syndrome, and Hyperprolactinemia: Who Started It? [PDF]
Case Reports in Rheumatology, 2016 We report a case of an 18-year-old girl who presented to our hospital with history of recurrent respiratory infections, amenorrhea, and symmetric polyarthritis.
Hussein Halabi, Israa Mulla
doaj +2 more sources
Unraveling the Complexities of Kartagener's Syndrome: A Case of Bronchiectasis, Isolated Dextrocardia, and Primary Ciliary Dyskinesia in an Adult With Chronic Respiratory Symptoms. [PDF]
Clin Case RepABSTRACT Kartagener's Syndrome (KS), a rare autosomal recessive disorder and a subset of Primary Ciliary Dyskinesia (PCD), is characterized by chronic sinusitis, bronchiectasis, and, in approximately 50% of cases, situs inversus. This condition arises from genetic mutations that impair motile cilia function, leading to defective mucociliary clearance ...
Khalil I, Abrar S, Ahmed ST, Hossain MI.
europepmc +2 more sources
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
doaj +2 more sources
Extracorporeal life support as rescue therapy in severe bronchiectasis with Kartagener’s syndrome [PDF]
Anaesthesiology Intensive Therapy, 2022 Riddhi Kundu +4 more
doaj +2 more sources
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
doaj +1 more source
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
doaj +2 more sources
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
doaj +1 more source
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
doaj +1 more source
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
doaj +1 more source
Kartagener’s syndrome: A case report [PDF]
Vojnosanitetski Pregled, 2016 Introduction. Kartagener’s syndrome is a recessive autosomal disease which is mainly seen to affect ciliary movement. The symptoms of the syndrome are the consequence of the defective motility of the cilia found in the respiratory tract and that results ...
Taušan Đorđe +2 more
doaj +1 more source