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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
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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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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 +2 more
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Síndrome de Kartagener em um cão (Canis lupus familiaris) da raça Cocker Spaniel Inglês [PDF]
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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Gomal Journal of Medical Sciences, 2014 Kartagener Syndrome is an autosomal recessive disorder, a subgroup of primary ciliary dyskinesia, characterized by a triad of bronchiectasis, sinusitis and situs inversus.
Khalid Shakeel Babar +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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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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Children, 2023 The goal of this manuscript is to present and summarize several rare pediatric syndromes (Zellweger syndrome, Kartagener syndrome, Prader-Willi syndrome, Schinzel-Giedion syndrome, Fanconi anemia, Joubert-Boltshauser syndrome, Poretti-Boltshauser ...
Laura M. Huisman +1 more
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Frontiers in Genetics, 2020 Introduction: Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease characterized by structural or functional motile cilia abnormalities. Up to 40 different genes seem, at the moment, to be involved in the pathogenesis of PCD.
Rossella Cannarella +7 more
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Kartagener syndrome complicated by pulmonary tuberculosis, HIV, and hepatitis B: a rare case report
The Egyptian Journal of BronchologyKartagener syndrome is a rare autosomal recessive genetic disorder characterized by situs inversus, bronchiectasis, and sinusitis. This case report describes a 23-year-old male presenting with chronic cough, shortness of breath, and dextrocardia on CXR ...
Thaodem Collin Singh +3 more
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