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Ablación de fibrilación auricular en paciente con dispositivo de oclusión septal interatrial
(Seguro Social de Salud (EsSalud), 2023-06-30)
Los dispositivos de oclusión del septo interatrial dificultan el abordaje transeptal para la ablación de la fibrilación auricular, por lo que es necesario contar con métodos de imagen que guíen con seguridad la punción ...
A novel TBX5 missense mutation (V263M) in a family with atrial septal defects and postaxial hexodactyly
(ELSEVIER IRELAND LTD, 2008)
Background: Congenital heart diseases are the most frequent birth defects and are commonly associated with skeletal malformations. Mutations in the TBX5 gene, a T-box transcription factor located on chromosome 12q24.1, ...
Hipoxemia recurrente y formen oval permeable. Unidad diagnóstica fácilmente inadvertida. Caso clínico
(Sociedad Médica de Santiago, 2020)
Patent foramen ovale (PFO) is a prevalent congenital septal atrial defect usually without pathological significance. In certain pathogenic situations, PFO can trigger episodes of recurrent hypoxemia, a specific condition ...
Phonocardiographic, radiological, and haemodynamic correlation in atrial septal defect
(BMJ Publishing Group, 1972)
Haemodynamic auscultatory, phonocardiographic, and haemodynamic radiological correlations were studied in 51 patients with proven atrial septal defect. A good correlation exists between the degree of left-to-right shunt ...
Recurrence of atrial septal defect in three generations
(Sociedade Brasileira de Cardiologia - SBC, 1999-08-01)
Beginning with a patient presenting with an atrial septal defect (ASD) of the secundum type, the genealogy was identified in four affected individuals who belonged to three successive generations of the same family. The ...
Horizontal right axillary minithoracotomy: aesthetic and effective option for atrial and ventricular septal defect repair in infants and toddlers
(Sociedade Brasileira de Cirurgia Cardiovascular, 2014-04-01)
Introduction:Congenital heart defects treatment shows progressive reduction in morbidity and mortality, however, the scar, resulting from ventricular (VSD) and atrial septal defect (ASD) repair, may cause discomfort. Right ...
Holt-Oram syndrome: novel TBX5 mutation and associated anomalous right coronary artery
(CAMBRIDGE UNIV PRESS, 2011)
The Holt-Oram syndrome was confirmed in an asymptomatic 36-year-old man by a novel TBX5-gene mutation (exon 8 acceptor splicing site, c.663-1G greater than A). Computed tomography showed an atrial septal defect and an ...
Gerbode defect and blunt chest trauma. Presentation of a case and literature reviewEl defecto de Gerbode y traumatismo torácico cerrado. Presentación de un caso y revisión de la literatura
(Universidad Nacional Mayor de San Marcos, Facultad de Medicina Humana, 2007)
Análisis de microdeleciones en 22q11 en pacientes colombianos con cardiopatía congénita no sindrómica.
Cardiac defects are the most frequent congenital malformations, with an incidence estimated between 4 and 12 per 1000 newborns. Their etiology is multifactorial and might be attributed to genetic predispositions and ...