Results 11 to 20 of about 1,525 (164)

Co-occurrence of Moyamoya syndrome and Kartagener syndrome caused by the mutation of DNAH5 and DNAH11: a case report [PDF]

open access: yesBMC 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   +2 more sources

Incidental imaging detection of Kartagener syndrome in a female: A case report [PDF]

open access: yesRadiology 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′s syndrome

open access: yesMedical Journal of Dr. D.Y. Patil University, 2013
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P K Satpathy   +2 more
doaj   +4 more sources

KARTAGENER SYNDROME

open access: yesGomal 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

Kartagener syndrome complicated by immunoglobulin A nephropathy [PDF]

open access: yesInternational Medical Case Reports Journal, 2018
Kentaro Oka,1 Taro Sugase,1 Tetsu Akimoto,1,2 Takuya Murakami,1 Izumi Nagayama,1 Miwa Kaneko,1 Maki Asakura,1 Ken Ohara,1 Osamu Saito,1 Daisuke Nagata1 1Division of Nephrology, Department of Internal Medicine, Jichi Medical University, Tochigi, Japan ...
Oka K   +9 more
doaj   +2 more sources

A case of Kartagener syndrome with rhinolalia clausa [PDF]

open access: yesThe 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

Actinomyces and Kartagener syndrome: Case report and literature review

open access: yesActa 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   +1 more source

Kartagener’s syndrome

open access: yesPan 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

Coronary artery bypass surgery in a patient with Kartagener syndrome: a case report and literature review

open access: yesJournal of Cardiothoracic Surgery, 2010
Kartagener syndrome consists of congenital bronchiectasis, sinusitis, and total situs inversus in half of the patients. A patient diagnosed with Kartagener syndrome was reffered to our department due to 3-vessel coronary disease.
Bougioukas Ioannis   +6 more
doaj   +1 more source

Nasopharyngeal carcinoma in a child with Kartagener`s syndrome

open access: yesThe Turkish Journal of Pediatrics, 2021
Background. Kartagener`s syndrome, a subgroup of primary ciliary dyskinesia, is characterized by situs inversus totalis, chronic sinusitis and bronchiectasis.
Buket Kara   +7 more
doaj   +1 more source

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