Results 11 to 20 of about 1,136,166 (186)

Kartagener syndrome complicated by immunoglobulin A nephropathy [PDF]

International Medical Case Reports Journal, 2018
Kentaro Oka,1 Taro Sugase,1 Tetsu Akimoto,1,2 Takuya Murakami,1 Izumi Nagayama,1 Miwa Kaneko,1 Maki Asakura,1 Ken Ohara,1 Osamu Saito,1 Daisuke Nagata1 1Division of Nephrology, Department of Internal Medicine, Jichi Medical University, Tochigi, Japan ...
Oka K, Sugase T, Akimoto T, Murakami T, Nagayama I, Kaneko M, Asakura M, Ohara K, Saito O, Nagata D   +9 more
doaj   +3 more sources

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

Acta 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

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

Journal 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, Mikroulis Dimitrios, Danner Bernhard, Lawal Lukman, Eleftheriadis Savvas, Bougioukas George, Didilis Vassilios   +6 more
doaj   +3 more sources

Kartagener syndrome: A review of three cases

Sahel Medical Journal, 2015
Kartagener's syndrome (KS) is an autosomal recessive subgroup of primary ciliary dyskinesia (PCD) which presents as sinusitis, bronchiectasis, and dextrocardia .The deficit in the coordination of ciliary motion results in mucus retention and recurrent ...
Avadhesh Kumar, Ajay Kumar Verma, Anand Kumar, Prashant Yadav, Ankit Bhatia, Saurabh Pahuja, Surya Kant   +6 more
doaj   +2 more sources

Co-occurrence of Moyamoya syndrome and Kartagener syndrome caused by the mutation of DNAH5 and DNAH11: a case report [PDF]

BMC Neurology, 2020
Background Kartagener syndrome is an autosomal recessive inherited disorder of primary ciliary dyskinesia. Moyamoya syndrome refers to a moyamoya angiopathy associated with other neurological and/or extra-neurological symptoms, or due to a well ...
Lili Zhang, Xungang Feng, Junhu Zhang, Yanlei Hao, Yuzhong Wang   +4 more
doaj   +2 more sources

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

Український 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, V.N. Nepomnyashchy, N.A. Kolesnyk   +2 more
doaj   +2 more sources

Kartagener Syndrome: A Rare Genetic Disorder

Journal 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

Atypical Kartagener syndrome in a 40-year-old woman: Computed Tomography findings of situs inversus with bronchiectasis and infertility [PDF]

Radiology Case Reports
Primary ciliary dyskinesia is a rare inherited disorder characterized by impaired mucociliary clearance leading to recurrent respiratory infections.
Yohannes Girma Zewdie, MD, Biniyam Beyene Tabor, MD, Ermias Fikru Yesuf, MD, Hana Yeshewas Genetirune, BSc   +3 more
doaj   +2 more sources

Kartagener′s syndrome

Medical Journal of Dr. D.Y. Patil University, 2012
Bronchiectasis may have varied etiologies. In patients presenting in middle or old age with bronchiectasis, congenital and hereditary causes of bronchiectasis are not commonly encountered. In majority of adult patients, bronchiectasis follows necrotizing
Pradip V Potdar, Mitali M Nayak, Aushutosh Chitnis   +2 more
doaj   +2 more sources

Incidental imaging detection of Kartagener syndrome in a female: A case report [PDF]

Radiology Case Reports
Kartagener syndrome is a rare ciliopathic genetic disorder characterized by a triad of chronic sinusitis, situs inversus, and bronchiectasis. The underlying pathophysiology involves reduced ciliary motility due to defects in ciliary structure and ...
Natasha Dhakal, MBBS, Prajwal Dahal, MD
doaj   +2 more sources