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Chromosome 22q11 deletion in a patient with pulmonary atresia, intact ventricular septum, and confluent branch pulmonary arteries
(Cambridge University Press, 2018)
In this study, we report a patient with pulmonary atresia with intact ventricular septum (PA/IVS), confluent pulmonary arteries supplied by an arterial duct, and chromosome 22q11.2 microdeletion. The 22q11.2 deletion ...
Atresia brônquica congênita: relato de dois casos. Contribuição da tomografia computadorizada ao diagnóstico
(Sociedade Brasileira de Pneumologia e Tisiologia, 2000-06-01)
Bronchial atresia is a rare, congenital anomaly characterized by the presence of bronchocele with distal hyperinflation. The authors report two cases of segmental bronchial atresia and describe the clinical and roentgenographic ...
Caso 6/2012: recém-nascido com atresia pulmonar, comunicação interventricular e duplo arco aórticoCase 6/2012: newborn with pulmonary atresia, ventricular septal defect and double aortic arch
(Sociedade Brasileira de Cardiologia - SBC, 2012)
Association of pulmonary atresia with intact ventricular septum and aortic valve stenosis. Prenatal diagnosis
(Sociedade Brasileira de Cardiologia - SBC, 2000-05-01)
A rare association of pulmonary atresia with an intact septum was diagnosed through echocardiography in a fetus 32 weeks of gestational age. The diagnosis was later confirmed by echocardiography of the newborn infant and ...
Proceso de atención de enfermería en un neonato con atresia pulmonar.
(Babahoyo: UTB-FCS, 2020, 2020)
Manejo percutáneo de hemoptisis severa en paciente post operada de cirugía de Fontan
(Seguro Social de Salud (EsSalud)PE, 2020-09-22)
Se presenta el caso de una paciente con antecedente de ventrículo único por atresia tricuspídea, doble vía de salida del ventrículo izquierdo e hipoplasia del anillo de la arteria pulmonar. La paciente fue tratada con ...
Sobrevida y resultados clínicos de los pacientes nacidos en Bogotá entre enero de 2009 y diciembre de 2013 con atresia esofágica
Determinar la sobrevida de los pacientes nacidos con atresia esofágica en Bogotá, además de los resultados clínicos de su tratamiento, comparando algunas variables con sus controles sanos.
Metodología: Se utilizó la base ...
Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases
(ELSEVIER IRELAND LTD, 2008)
Background: Tetralogy of Fallot (TOF) is a congenital conotruncal heart defect commonly found in DiGeorge (DGS) and velocardiofacial (VCFS) syndromes. The deletion of chromosome 22q11 has also been demonstrated in sporadic ...