Results 281 to 290 of about 89,678 (332)
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Distal aortic remodeling using endovascular repair in acute DeBakey I aortic dissection.
Seminars in Thoracic and Cardiovascular Surgery, 2009DeBakey type I aortic dissections pose significant challenges in operative and long-term management of the arch and distal thoracic aorta. Concerns regarding management of complex tears extending to the arch and descending thoracic aorta, malperfusion ...
N. Desai, A. Pochettino
semanticscholar +1 more source
The EOG and the ERG in the Aortic Arch Syndrome
1983The authors studied the EOG and the ERG in patients with ocular pathology related to the aortic arch syndrome; both records, the EOG and the ERG showed abnormalities. The importance of the EOG is emphasized by the authors as a clinical test to recognize the early choroidal vascular pathology in these cases and to understand better the associated ...
J. Ribeiro-da-Silva +1 more
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Pediatric Pathology, 1984
The most common multiple anomaly complex with pulmonary isomerism and congenital heart disease is the Ivemark asplenia syndrome.’ Regular features of this disorder include: pulmonary isomerism of right lung type, with three lobar bronchi in each lung ...
B. Landing
semanticscholar +1 more source
The most common multiple anomaly complex with pulmonary isomerism and congenital heart disease is the Ivemark asplenia syndrome.’ Regular features of this disorder include: pulmonary isomerism of right lung type, with three lobar bronchi in each lung ...
B. Landing
semanticscholar +1 more source
Cogan's syndrome with aortitis, aortic regurgitation, and aortic arch vessel stenoses
The Annals of Thoracic Surgery, 1991Cogan's syndrome of interstitial keratitis and vestibuloauditory dysfunction is rare. Systemic vasculitic manifestations occur, and 10% of patients with this syndrome have aortic valvular disease. A patient with Cogan's syndrome is presented who had aortitis of the ascending thoracic aorta, severe aortic valve regurgitation, orificial stenosis of the ...
Andrew D. Cochrane, James Tatoulis
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Aortic Arch Management During Acute and Subacute Type A Aortic Syndromes.
Annals of Thoracic Surgery, 2022Parthavkumar Patel +6 more
semanticscholar +1 more source
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
Developmental Disabilities Research Reviews, 2008Specific types and subtypes of cardiac defects have been described in children with 22q11.2 deletion syndrome as well as in other genetic syndromes. The conotruncal heart defects occurring in patients with 22q11.2 deletion syndrome include tetralogy of ...
A. Carotti +5 more
semanticscholar +1 more source
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
openaire +3 more sources
American journal of medical genetics, 1995
We present the largest single series of cases (n = 5) of penoscrotal transposition (PST) with carefully documented nongenitourinary/anal anomalies, none of which fell into categories of known syndromes, associations, sequences or chromosome disorders ...
S. Parida +3 more
semanticscholar +1 more source
We present the largest single series of cases (n = 5) of penoscrotal transposition (PST) with carefully documented nongenitourinary/anal anomalies, none of which fell into categories of known syndromes, associations, sequences or chromosome disorders ...
S. Parida +3 more
semanticscholar +1 more source