Results 11 to 20 of about 2,234 (198)

Kartagener syndrome [PDF]

open access: yesInternational Journal of General Medicine, 2011
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
doaj   +11 more sources

Actinomyces and Kartagener syndrome: Case report and literature review [PDF]

open access: yesActa Médica Peruana, 2022
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
doaj   +2 more sources

Retinal pigment epithelium changes in Kartagener syndrome

open access: yesAmerican Journal of Ophthalmology Case Reports, 2018
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
doaj   +2 more sources

Acute Appendicitis in Patients with Kartagener Syndrome

open access: yesCase Reports in Surgery, 2020
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
doaj   +2 more sources

Pulmonary mucoepidermoid carcinoma arising in a patient with Kartagener syndrome

open access: yesBMC Pulmonary Medicine, 2020
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
doaj   +2 more sources

Coronary artery bypass surgery in a patient with Kartagener syndrome: a case report and literature review [PDF]

open access: yesJournal of Cardiothoracic Surgery, 2010
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
doaj   +3 more sources

Kartagener Syndrome: A Rare Genetic Disorder

open access: yesJournal of Nepal Medical Association, 2009
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
doaj   +2 more sources

THE COMBINATION OF KARTAGENER SYNDROME WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS: CASE REPORT

open access: yesУкраїнський Журнал Нефрології та Діалізу, 2015
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
doaj   +2 more sources

EARLY DIAGNOSIS AND TREATMENT IN PATIENT WITH A PRIMARY CILIARY DYSKINESIA (KARTAGENER SYNDROME): CASE REPORT [PDF]

open access: yesАрхивъ внутренней медицины, 2018
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
doaj   +2 more sources

Kartagener syndrome: A case report

open access: yesCanadian Journal of Respiratory Therapy, 2021
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
doaj   +2 more sources

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