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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 +4 more
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
doaj +2 more sources
A Case Report of Kartagener Syndrome [PDF]
The Journal of Qazvin University of Medical Sciences, 2020 Primary Ciliary Dyskinesia (PCD) and Kartagener Syndrome (KS) are rare genetic disorders. PCD occurs in patients with recurrent sino-pulmonary infection, dextrocardia, chronic vasomotor rhinitis, and bronchiectasis.
Mahnaz Moradi +3 more
doaj +2 more sources
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
doaj +1 more source
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 +2 more sources
Videothoracoscopic lobectomy for bronchiectasis and extrapulmonary sequestration in a case Kartagener syndrome with pectus excavatum. [PDF]
Turk Gogus Kalp Damar Cerrahisi Derg, 2021 Kartagener syndrome is a rare condition. A 21-year-old female patient was under follow-up for five years by the chest diseases clinic due to recurrent cough, sputum production and wheezing, and she was diagnosed with Kartagener syndrome.
Aydoğmuş Ü.
europepmc +2 more sources
Kartagener′s syndrome in a fertile male - An uncommon variant
Lung India, 2006 Primary ciliary dyskinesia, with Kartagener′s syndrome as one of the subsets, is an autosomal recessive disorder with significant genetic heterogeneity.
Barthwal M
doaj +1 more source
Kartagener syndrome: Case report. [PDF]
, 2021 Kartagener’s syndrome is an autosomal recessive disease, characterized by primary ciliary dyskinesia, which consists of ciliated cell dysfunction. This is the cause of the manifestation of the respiratory symptomatology that presents this syndrome-cough,
Fajardo, German +3 more
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KARTAGENER SYNDROME: A CASE REPORT [PDF]
, 2018 Kartagener syndrome is a rare genetic disorder which includes a triad of bronchiectasis, chronic sinusitis, and situs inversus. Primary ciliary dyskinesia (PCD) can be one of the causes of the above symptoms in this syndrome.
Najafi, Samane +2 more
core +3 more sources
Pan African Medical Journal, 2018 A 29-year-old non-smoker male with a history of chronic cough, and recurrent pneumonia, sinusitis and otomastoiditis was admitted to the emergency room with a 3-day history of headache, cough productive and dyspnea. Positive findings on physical examination included heart sounds in the right side of his chest and pain on palpation and percussion of the
Rodolfo Mendes Queiroz +1 more
openaire +3 more sources