Results 151 to 160 of about 1,222,414 (189)
Some of the next articles are maybe not open access.
Chest, 1972
Clinical observations of 19 patients with Kartagener's syndrome seen during the past 25 years support the concept of congenital functional or anatomic defects in the mucociliary epithelium and its supporting structures. The case of a woman with this syndrome, who is alive at the age of 72 years, is detailed to suggest that, with reasonable medical ...
R D, Miller, M B, Divertie
openaire +4 more sources
Clinical observations of 19 patients with Kartagener's syndrome seen during the past 25 years support the concept of congenital functional or anatomic defects in the mucociliary epithelium and its supporting structures. The case of a woman with this syndrome, who is alive at the age of 72 years, is detailed to suggest that, with reasonable medical ...
R D, Miller, M B, Divertie
openaire +4 more sources
EuroIntervention, 2007
289 A 46-year-old man with Kartagener’s Syndrome (primary ciliary diskinesia, autosomal recessive disorder with dextrocardia, situs inversus, bronchiectasis and paranasal sinusitis) presented with new onset angina. Coronary arteriography revealed severe three-vessel disease with occluded left anterior descending and circumflex coronary arteries. Due to
Annick, Weustink +3 more
openaire +2 more sources
289 A 46-year-old man with Kartagener’s Syndrome (primary ciliary diskinesia, autosomal recessive disorder with dextrocardia, situs inversus, bronchiectasis and paranasal sinusitis) presented with new onset angina. Coronary arteriography revealed severe three-vessel disease with occluded left anterior descending and circumflex coronary arteries. Due to
Annick, Weustink +3 more
openaire +2 more sources
Archives of Surgery, 1959
The purpose of this paper is to report a case of Kartagener's syndrome. The occurrence of situs inversus and bronchiectasis was first noted in 1904 by Siewert,4who described a case of situs inversus in a 20-year-old youth. The triad of situs inversus, bronchiectasis, and paranasal sinusitis has been more fully described by Adams and Churchill ...
B G, STREETE, F E, STULL
openaire +2 more sources
The purpose of this paper is to report a case of Kartagener's syndrome. The occurrence of situs inversus and bronchiectasis was first noted in 1904 by Siewert,4who described a case of situs inversus in a 20-year-old youth. The triad of situs inversus, bronchiectasis, and paranasal sinusitis has been more fully described by Adams and Churchill ...
B G, STREETE, F E, STULL
openaire +2 more sources
Kartagener's Syndrome in Childhood
Archives of Pediatrics & Adolescent Medicine, 1971Kartagener's syndrome is manifest by the association of sinusitis, situs inversus, and bronchiectasis. We treated three children with Kartagener's syndrome, two of them sisters. Respiratory symptoms began in infancy in all three patients. In case 1, a normal bronchogram was seen at 6 years of age; a second bronchogram at 13 years was grossly abnormal ...
J V, Hartline, P S, Zelkowitz
openaire +2 more sources
Inheritance of Kartagener syndrome
American Journal of Medical Genetics, 1981AbstractThe surmised autosomal recessive inheritance of situs inversus of Kartagener syndrome is re‐examined on the hypothesis that the homozygous state replaces lateralization of the viscera in normal ontogeny by an indifferent lateralization. The segregation ratio in the progeny of two carrier parents (if there were no ascertainment bias) would then ...
A, Moreno, E A, Murphy
openaire +2 more sources
Kartagener's Syndrome—A Reappraisal
Acta Oto-Laryngologica, 1978Congenital lack of dynein arms in cilia has recently been associated with Kartagener's syndrome. Ultrastructural findings from six patients with chronic stagnant secretion in the respiratory tract are briefly reported. Only one of the patients had the complete syndrome.
openaire +2 more sources
JAMA, 1982
Kartagener's syndrome, characterized by situs inversus, paranasal sinusitis, and bronchiectasis, is part of a more generalized syndrome characterized by sterility in men, chronic bronchitis or bronchiectasis, chronic sinusitis, and chronic otitis media; it is referred to as the immotile-cilia syndrome.
J H, Woodring, J M, Royer, D, McDonagh
openaire +1 more source
Kartagener's syndrome, characterized by situs inversus, paranasal sinusitis, and bronchiectasis, is part of a more generalized syndrome characterized by sterility in men, chronic bronchitis or bronchiectasis, chronic sinusitis, and chronic otitis media; it is referred to as the immotile-cilia syndrome.
J H, Woodring, J M, Royer, D, McDonagh
openaire +1 more source
American family physician, 1991
Kartagener's syndrome is characterized by situs inversus, chronic paranasal sinusitis and bronchiectasis. The pathogenesis of this rare condition is an ultrastructural defect that results in immotile cilia. Radiologic features may include findings consistent with bronchiectasis.
T B, Kinney, S A, DeLuca
openaire +1 more source
Kartagener's syndrome is characterized by situs inversus, chronic paranasal sinusitis and bronchiectasis. The pathogenesis of this rare condition is an ultrastructural defect that results in immotile cilia. Radiologic features may include findings consistent with bronchiectasis.
T B, Kinney, S A, DeLuca
openaire +1 more source