Results 61 to 70 of about 3,617 (177)

Deleción 22q11.2 en pacientes con defecto cardiaco conotruncal y fenotipo del síndrome de la deleción 22q11.2 [PDF]

open access: yes, 2009
BACKGROUND: The 22q11.2 deletion syndrome is the most frequent human microdeletion syndrome. The phenotype is highly variable, being characterized by conotruncal heart defect, facial dysmorphisms, velopharyngeal insufficiency, learning difficulties and ...
Belangero, Sintia Iole   +5 more
core   +3 more sources

Anesthetic management for surgery of esophagus atresia in a newborn with Goldenhar's syndrome

open access: yesBrazilian Journal of Anesthesiology, 2015
Background and objectives: Goldenhar's syndrome is a polymalformative condition consisting of a craniofacial dysostosis that determines difficult airway in up to 40% of cases.
Rosana Guerrero-Domínguez   +3 more
doaj   +1 more source

The Surgical Face of a Neonatal Intensive Care Unit [PDF]

open access: yes, 2010
Introdução e objectivos: O Hospital de Dona Estefânia é um hospital pediátrico com Área de Cirurgia Pediátrica e uma Maternidade da Apoio Perinatal Diferenciado. O objectivo deste estudo prospectivo histórico é analisar a população de recém-nascidos (RN)
Casella, P   +3 more
core  

Operação de Blalock-Taussig modificada para o tratamento paliativo de cardiopatias congênitas com hipofluxo pulmonar Blalock-Taussig operation for palliative treatment of congenital heart disease with low pulmonary flow

open access: yesBrazilian Journal of Cardiovascular Surgery, 1995
De janeiro de 1990 a novembro de 1994, 72 pacientes portadores de cardiopatias congênitas com hipofluxo pulmonar foram submetidos à operação de Blalock-Taussig.
Miguel A Maluf   +8 more
doaj  

Toracoplastia expansiva en el tratamiento de la escoliosis congénita torácica con malformaciones vertebrales asociadas a fusión costal [PDF]

open access: yes, 2009
Se presenta el caso clínico de un paciente varón de 3 años de edad con escoliosis congénita torácica en el contexto de un síndrome de VACTERL, que presentaba defectos múltiples de segmentación vertebral con fusión costal asociada, en el que se realizó ...
Bas Hermida, Teresa   +3 more
core  

Pulmonary Atresia with Intact Ventricular Septum and Absence of Tricuspid Valve. A Report of Four Cases

open access: yesMedisur, 2013
Pulmonary atresia with intact ventricular septum suggests a simple congenital heart malformation. However, nothing could be further from the truth. Among the morphological peculiarities of this condition, the presence of congenitally unguarded tricuspid ...
Adel E. González Morejón   +2 more
doaj   +2 more sources

Congenital Lobar Emphysema: A Multilobar Presentation [PDF]

open access: yes, 2011
O enfisema lobar congénito é umamalformação rara do tracto respiratório inferior detectada habitualmente nos primeiros meses de vida. Apresenta-se o caso de um lactente, do sexo masculino, de dois meses de idade, internado por suspeita de pneumonia, no ...
Alves, R   +5 more
core  

A novel adjustable pulmonary artery banding system for hypoplastic left heart syndrome [PDF]

open access: yes, 2007
OBJECTIVE: Hypoplastic left heart syndrome remains a challenge for worldwide surgeons. Initial palliation employing bilateral pulmonary artery banding along with ductal stent implantation and atrial septostomy has been proposed as an alternative approach.
Assadi, Renato Samy   +7 more
core   +3 more sources

Cianosis neonatal [PDF]

open access: yes, 2014
PROTOCOLOS TERAPEUTICOS. CIANOSIS NEONATAL. 1. CONCEPTO Se considera cianosis a la coloración azulada de la piel o de las mucosas secundaria a un oscurecimiento sanguíneo producido por un aumento de la hemoglobina reducida (principalmente HbFe ++) a ...
Pastor Durán, Xavier
core  

Anastomose cavo-pulmonar total sem uso de material protético

open access: yesBrazilian Journal of Cardiovascular Surgery, 1998
Objetivo: Demonstrar a viabilidade na feitura de túnel cava inferior-cava superior com retalho da parede atrial direita, evitando o emprego de material protético.
Valdester C. PINTO Jr.   +12 more
doaj   +1 more source

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