Results 21 to 30 of about 1,525 (164)
Хірургія дитячого віку, 2018 The rarity of Kartagener syndrome, as well as the presence of structural malformative changes associated with the progressive development of granulomatous bronchiolitis, was considered appropriate for the presentation of a clinical case with unfavorable ...
S. Babuci +3 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 +2 more
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Bronchiolitis in Kartagener's syndrome [PDF]
European Respiratory Journal, 1999 The association of diffuse bronchiolitis in patients with Kartagener's syndrome (KS) has not been reported previously. The aim of this study was to present the morphological characteristics of bronchiolitis in patients with KS. Eight patients (four males, four females; mean age 37.9+/-18.7 yrs), clinically diagnosed as KS with the classical triad of ...
S, Homma +7 more
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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 +4 more
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Right Bochdalek Hernia Associated with Kartagener Syndrome: Developmental and Clinical Observations
European Journal of Pediatric Surgery Reports, 2013 We present a novel case of the association of right-sided Bochdalek hernia, a diaphragmatic life-threatening malformation, and Kartagener syndrome, which is characterized by congenital bronchiectasis, chronic sinusitis, and situs inversus.
Carmelo Romeo +4 more
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The Pan African Medical Journal, 2019 Le syndrome de Kartagener est une entité particulière parmi les dyskinésies ciliaires primitives (DCP) caractérisée par une triade clinique: sinusite, bronchectasie et situs inversus complet ou incomplet. C'est une maladie congénitale rare à transmission
Amadou Doumbia +4 more
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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 +6 more
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Síndrome de Kartagener em um cão (Canis lupus familiaris) da raça Cocker Spaniel Inglês
Arquivo Brasileiro de Medicina Veterinária e Zootecnia, 2011 Kartagener is syndrome is a rare disorder described in dogs determined by the triad situs inversus totalis, chronic sinusitis, and bronchial disease. The clinical signs of chronic respiratory and other less common presentations (such as hydrocephalus and
P. Souza Junior +2 more
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Molecular Genetics &Genomic Medicine, Volume 14, Issue 7, July 2026.We report pseudo‐dominant PCD inheritance in a Chinese family due to novel DNAAF1 mutations. Affected members across two generations showed significant variability in lung disease progression and visceral arrangement. ABSTRACT Background Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disorder typically inherited in an autosomal ...
Zhuoyao Guo +3 more
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A woman with recurrent respiratory tract infections
The Pan African Medical Journal, 2020 A 76-year-old Caucasian woman who has been repeatedly hospitalized with recurrent respiratory tract infections, presented to the emergency department with fever and productive cough during the last 24 hours.
Petros Ioannou
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