Results 11 to 20 of about 2,234 (198)
Nedaa Skeik1–3, Fadi I Jabr41Mayo Clinic, Rochester, MN, USA; 2Dartmouth Medical School, Hannover, NH, USA; 3New York Medical College, New York, NY, USA; 4Horizon Medical Center, Hospital Medicine, Dickson, TN, USAAbstract: Kartagener syndrome ...
Nedaa Skeik, Fadi I Jabr
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Actinomyces and Kartagener syndrome: Case report and literature review [PDF]
Kartagener syndrome, which is part of the subgroup of the primary ciliary dyskinesias, predisposes to recurrent respiratory tract infections due to Haemophilus influenzae, Staphylococcus aureus and Streptococcus pneumoniae.
Carlos Mauricio Martinez Montalvo
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Retinal pigment epithelium changes in Kartagener syndrome
Purpose: We present the first case in the literature of a patient with Kartagener syndrome and ocular findings of nonexudative age-related macular degeneration. Observations: A 55-year-old woman with Kartagener syndrome and chronic angle closure glaucoma
Maria D. Garcia +4 more
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Acute Appendicitis in Patients with Kartagener Syndrome
Situs inversus totalis is a congenital syndrome characterized by a total left-right transposition of all abdominal and thoracic organs. It may be associated with chronic respiratory conditions such as sinusitis and bronchiectasis, composing the ...
Pedro Nogarotto Cembraneli +4 more
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Pulmonary mucoepidermoid carcinoma arising in a patient with Kartagener syndrome
Background Kartagener syndrome, an autosomal recessive disorder with a triad of chronic sinusitis, bronchiectasis, and situs inversus, is characterized by recurrent respiratory tract infections and chronic inflammation of the lung.
Yoshiaki Nagai +8 more
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Coronary artery bypass surgery in a patient with Kartagener syndrome: a case report and literature review [PDF]
Kartagener syndrome consists of congenital bronchiectasis, sinusitis, and total situs inversus in half of the patients. A patient diagnosed with Kartagener syndrome was reffered to our department due to 3-vessel coronary disease.
Bougioukas Ioannis +6 more
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Kartagener Syndrome: A Rare Genetic Disorder
Kartagener Syndrome is a rare autosomal recessive disorder consisting of triad of sinusitis, bronchiectasis and situs inversus with dextrocardia. It is the subset of disorder called primary ciliary dyskinesia in which the cilia have abnormal structure ...
Kunjan Shakya
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THE COMBINATION OF KARTAGENER SYNDROME WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS: CASE REPORT
Kartagener syndrome - a form ofprimary ciliary dyskinesia, which combines situs inversus totalis or only dextrocardia with the defeat of the respiratory system.
E.V. Burdeina +2 more
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EARLY DIAGNOSIS AND TREATMENT IN PATIENT WITH A PRIMARY CILIARY DYSKINESIA (KARTAGENER SYNDROME): CASE REPORT [PDF]
Primary ciliar dyskinesia is а rare orphan disease known for its multiple and variable symptoms caused by the marked genetic heterogenity beyond. As per the abundant symptoms in pediatric patients, a frequent inflammatory diseases of both upper and lower
I. V. Rybakova +4 more
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Kartagener syndrome: A case report
Kartagener syndrome is a rare, autosomal recessive genetic disorder that causes defects in the action of ciliary movement, comprises of triad situs inversus, chronic sinusitis, and bronchiectasis.
Ibrahim Rahaf, Daood Huda
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