Results 211 to 220 of about 7,571 (244)
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Interruption of aortic arch and hypoplastic left heart syndrome
Pediatric Cardiology, 1995Interruption of the aortic arch and hypoplastic left heart syndrome in the same patient is exceptional. In the combined collections of the Registry of Cardiovascular Disease (St. Paul, Minnesota, U.S.A.) and the Registry of Congenital Heart Defects of the Rijksuniversiteit Gent (Gent, Belgium) three specimens were found with this unusual combination ...
Jesse E. Edwards +5 more
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Absent pulmonary valve syndrome with interrupted aortic arch
The Annals of Thoracic Surgery, 1998A surgically treated case of absent pulmonary valve syndrome associated with type B interrupted aortic arch is presented. The presence of a restrictive ductus arteriosus promoted the development of a collateral circulation between ascending and descending thoracic aorta, allowing the child to remain clinically stable after birth.
D. Wilson +4 more
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Aortic Arch Abnormality in a Patient with Klippel-Feil Syndrome
Vascular, 2006We present a case of a 43-year-old female with headaches, progressive paresthesias of the upper extremities, and vertigo. Ultrasonography could not visualize the left internal carotid artery (ICA). Magnetic resonance imaging (MRI) showed complete fusion of the C5, C6, and C7 levels, representing Klippel-Feil deformity.
Jihad Abbas +3 more
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Congenital subclavian steal syndrome with anomaly of the aortic arch
Surgical Neurology, 1993A case of congenital subclavian steal syndrome associated with an anomalous right-sided aorta is reported. A 41-year-old man complaining of vertigo and a loss of consciousness was admitted. Physical examination revealed a blood pressure differential between the arms that was 20 mm Hg less in the left.
Shoichi Inagawa +5 more
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Giant-cell Arteritis Producing an Aortic Arch Syndrome
Annals of Internal Medicine, 1967Excerpt Patients with giant-cell arteritis (temporal or cranial arteritis) have long been recognized to have involvement of arteries other than the temporal arteries.
Gene G. Hunder +2 more
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Echocardiography, 2015
PHACE is a rare congenital neurocutaneous syndrome where posterior fossa malformations, hemangiomas, cerebrovascular anomalies, aortic arch anomalies, cardiac defects, and eye abnormalities are variably associated. We describe the prenatal detection and the postnatal course of a child with PHACE syndrome with a unique type of aortic arch anomaly ...
Chiappa E. +5 more
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PHACE is a rare congenital neurocutaneous syndrome where posterior fossa malformations, hemangiomas, cerebrovascular anomalies, aortic arch anomalies, cardiac defects, and eye abnormalities are variably associated. We describe the prenatal detection and the postnatal course of a child with PHACE syndrome with a unique type of aortic arch anomaly ...
Chiappa E. +5 more
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The Value of Aortic Valve and Aortic Arch Imaging in the Identification of Genetic Syndromes
Echocardiography, 1996Echocardiographers imaging the aortic valve, root, and arch may observe coincidental extracardiac malformations, unusual facial features or body habitus, and/or mental or growth retardation. The pattern of anomalies may indicate a previously unrecognized genetic malformation syndrome.
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Syndrome of constricting double aortic arch in infancy
The Journal of Pediatrics, 1939Summary An instance of double aortic arch constricting trachea and esophagus is described, along with six others collected from the literature. These cases showed a common and more or less characteristic syndrome, which consisted of stridorous breathing, dysphagia, chronic cough, susceptibility to bronchopneumonia, head retraction, malnutrition, and ...
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The aortic arch syndrome of Takayasu
American Heart Journal, 1958William Dubilier +2 more
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