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Kartagener syndrome with minimal change disease: a case report [PDF]

Journal of Medical Case Reports
Background Kartagener syndrome is characterized by chronic sinusitis, bronchiectasis, and total visceral transposition. While there are few reports of Kartagener syndrome combined with kidney disease, there are none that specifically report Kartagener ...
Qun Huang, Junjun Luan, Hua Zhou
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Kartagener syndrome in a young Ethiopian boy: a case report [PDF]

Journal of Medical Case Reports
Introduction Kartagener syndrome is a subset of a larger group of ciliary motility disorders called primary ciliary dyskinesias. The syndrome includes the clinical triad of chronic sinusitis, bronchiectasis, and situs inversus.
Habtamu Mesele Gebray, Addisu Liknaw Chekol, Samuel Addis Mihiretie, Abayneh Tunta Boye, Zeru Seyoum Wendimagegn, Zenebe Daniel Getachew   +5 more
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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
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Kartagener syndrome rarely revealed by chronic diarrhea in an adult: A case report [PDF]

Radiology Case Reports
Kartagener syndrome, a subset of primary ciliary dyskinesia, is characterized by the clinical triad of chronic sinusitis, cylindric bronchiectasis, and situs inversus totalis. Gastrointestinal manifestations are rarely described.
Saleck Choumad, MD, Hind Qajia, MD, Chaimae Abourak, MD, Ahmed Ebedda, MD, Itimad Nassar, PhD, Kaoutar Imrani, PhD   +5 more
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EARLY DIAGNOSIS AND TREATMENT IN PATIENT WITH A PRIMARY CILIARY DYSKINESIA (KARTAGENER SYNDROME): CASE REPORT [PDF]

Архивъ 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, I. V. Koroleva, A. V. Khizhniak, O. V. Sidorovich, S. Iu. Elizarova   +4 more
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Kartagener syndrome with partial anomalous pulmonary venous drainage: a case report [PDF]

Journal of Medical Case Reports
Background Kartagener syndrome, defined by situs inversus, bronchiectasis, and chronic sinusitis. This condition rarely coexists with cardiac anomalies.
Dwika Rasyid Firmanda, Alisia Yuana Putri, Cornelia Ghea, Asiyah Nurul Fadila, Emil Prabowo, Vammy Valentine, Fauzan Hamadah   +6 more
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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
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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
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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

Kartagener syndrome with pulmonary tuberculosis in a fertile male: A rare co-existence

Journal of Medical Sciences, 2015
Kartagener syndrome (KS), a subset of primary ciliary dyskinesia, is an autosomal recessive disorder with variable phenotypic expressions. Males with this syndrome are usually infertile.
Manoj Kumar Panigrahi, King Herald Kisku
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