Results 1 to 10 of about 1,929 (174)
Pulmonary mucoepidermoid carcinoma arising in a patient with Kartagener syndrome [PDF]
BMC 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 +4 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 +4 more
doaj +4 more sources
Novel compound heterozygous mutations of DNAH5 identified in a pediatric patient with Kartagener syndrome: case report and literature review [PDF]
BMC Pulmonary Medicine, 2021 Background Kartagener syndrome is a subtype of primary ciliary dyskinesia that may exhibit various symptoms including neonatal respiratory distress and frequent infections of the lung, sinus and middle ear because of the impaired function of motile cilia.
Lina Wang +8 more
doaj +4 more sources
A case of Kartagener syndrome with rhinolalia clausa [PDF]
The Pan African Medical Journal, 2016 Kartagener syndrome is an autosomal recessive genetic ciliary disorder comprising of a classic triad of sinusitis, situs inversus and bronchiectasis. It's the one of primary ciliary dyskinesia disorders with manifestations present from childhood.
Mohammed Raoufi +10 more
doaj +4 more sources
Incidental imaging detection of Kartagener syndrome in a female: A case report [PDF]
Radiology Case ReportsKartagener 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 +3 more sources
Actinomyces and Kartagener syndrome: Case report and literature review
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 +3 more sources
International 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 +9 more sources
Kartagener syndrome: A case report [PDF]
Canadian 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
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 +2 more
doaj +3 more sources
Kartagener syndrome with minimal change disease: a case report [PDF]
Journal of Medical Case ReportsBackground 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
doaj +2 more sources