Results 21 to 30 of about 1,929 (174)

Identification of Pathogenic Mutations and Investigation of the NOTCH Pathway Activation in Kartagener Syndrome [PDF]

Frontiers in Genetics, 2019
Primary ciliary dyskinesia (PCD), a rare genetic disorder, is mostly caused by defects in more than 40 known cilia structure-related genes. However, in approximately 20–35% of patients, it is caused by unknown genetic factors, and the inherited ...
Yongjian Yue, Qijun Huang, Peng Zhu, Pan Zhao, Xinjuan Tan, Shengguo Liu, Shulin Li, Xuemei Han, Linling Cheng, Bo Li, Yingyun Fu   +10 more
doaj   +2 more sources

Kartagener syndrome complicated by immunoglobulin A nephropathy [PDF]

International 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, Sugase T, Akimoto T, Murakami T, Nagayama I, Kaneko M, Asakura M, Ohara K, Saito O, Nagata D   +9 more
doaj   +2 more sources

Kartagener Syndrome in Two Siblings: A Familial Case Report With Phenotypic Variability and Destroyed Lung Syndrome as a Rare Complication [PDF]

Cureus
El Khachine I, Boukharta A, Zahraoui R, El Bourkadi J, Soualhi M.   +4 more
europepmc   +3 more sources

Kartagener syndrome with pectus excavatum and upper lobar bronchiectasis. [PDF]

Radiol Case Rep
Khan ZS, Saini SK, Chua WJ, Jacky Liao HT, Manikkam S.   +4 more
europepmc   +2 more sources

Kartagener syndrome [PDF]

QJM: An International Journal of Medicine, 2017
Wayland Wang
openalex   +3 more sources

A rare case report: Left middle lobectomy in recurrent hemoptysis and chest infections of Kartagener syndrome patient. [PDF]

Int J Surg Case Rep
Fatimi AS, Wahab R, Mir F, Iqbal S, Fatimi SH.   +4 more
europepmc   +2 more sources

Kartagener syndrome

, 2020
Mostafa El-Feky
openalex   +2 more sources

Nasopharyngeal carcinoma in a child with Kartagener`s syndrome

The 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, Nusret Seher, Meryem İlkay Eren-Karanis, Mustafa Koplay, Hasibe Artaç, Mehmet Koç, Ahmet Okay Çağlayan, Yavuz Köksal   +7 more
doaj   +1 more source

Incidental Diagnosis of Situs Inversus Totalis in a 45-Year-Old Male Who Presented With Acute Asthma Exacerbation: A Case Report and Brief Literature Review. [PDF]

Clin Case Rep
ABSTRACT Incidental situs inversus totalis (SIT) requires thorough anatomical mapping to exclude associated syndromes (e.g., Kartagener) and congenital anomalies. Early identification, patient education on mirrored anatomy, and multidisciplinary coordination are essential to prevent iatrogenic errors during future interventions, even in asymptomatic ...
Bayisa RG, Baharu LM, Abafogi MM, Bonsa YB, Shukri MK, Woyimo TG.   +5 more
europepmc   +2 more sources

Kartagener’s syndrome

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, Fred Bernardes Filho   +1 more
openaire   +3 more sources