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transposition of great vessels/seizures
Il collegamento viene salvato negli appunti
11 risultati
[Morgagni-Adams-Stokes-seizures in a young patient with corrected transposition of the great vessels].
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Predictors of developmental outcomes in children with complete transposition.
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Cognitive, functional, educational achievement and behavioural measures were employed to assess neurobehavioral status in 57 of 60 participants who were initially enrolled in the Baltimore-Washington Infant Study, and who survived surgical correction of complete transposition (concordant
Results of Fontan operation in patients with congenitally corrected transposition of great arteries†.
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OBJECTIVE
The purpose of this study was to examine the outcome after the Fontan operation in patients with congenitally corrected transposition of great arteries with ventricular septal defect and pulmonary stenosis (ccTGA-VSD-PS).
METHODS
Patient- and procedure-related variables were analysed in 23
A Case of Congenitally Corrected Transposition of Great Arteries: An Infrequent Happenstance.
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Congenitally corrected transposition of the great arteries (CCTGA) is rare form of congenital heart diseases. It may be present with or without associated anomalies. Patients with CCTGA are usually diagnosed at early stages of life due to associated anomalies, but they may even remain asymptomatic
Neurodevelopmental outcome related to cerebral risk factors in children after neonatal arterial switch operation.
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BACKGROUND
Neurodevelopmental outcome after neonatal arterial switch operation for complete transposition of the great arteries is an important topic needing prospective assessment.
METHODS
A group of 33 unselected children (3.0 to 4.6 years) operated on as neonates with combined deep hypothermic
Serum lactate as mortality and morbidity marker in infants after Jatene's operation.
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OBJECTIVE
To assess the morbidity and mortality after Jatene's operation using lactate as the main marker.
METHODS
We performed a historical cohort with infants admitted in a pediatric intensive care unit during 1995 to 2005 who underwent this surgery. We assessed the preoperative, immediate (IPD),
Cardiac malformations are increased in infants of mothers with epilepsy.
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We aimed to ascertain the prevalence of cardiac malformation (CM) and its association with antenatal exposure to an antiepileptic drug (AED) in infants of mothers with epilepsy (IMEs). Women with epilepsy (WWE) are enrolled in Kerala Registry of Epilepsy and Pregnancy (KREP) in the prepregnancy or
Anesthesia for arterial switch operation in simple transposition of the great arteries: experience at Siriraj Hospital.
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Anesthetic management of cardiac patients with complete transposition of the great arteries (TGA) undergoing arterial switch operation (ASO) is challenging. The anesthetic course and perioperative problems were studied. A prospective data collection study of 87 patients was performed between January
Prostaglandin E1: first stage palliation in neonates with congenital cardiac defects.
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E-type prostaglandins (PGE1) can effectively maintain the patency of the ductus arteriosus in neonates. Its use, therefore can be life saving in infants born with ductus dependent congenital heart disease. Although PGE1 is available for over two decades in western world, it has been introduced in
Neurocutaneous melanosis with transposition of the great arteries and renal agenesis.
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Neurocutaneous melanosis (NCM) is rare and is characterized by the proliferation of melanocytes in the central nervous system. A 6-day-old infant boy was referred to our department with giant congenital melanocytic nevi and convulsions. On physical examination the patient had a giant black-brown
Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation.
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A decade after the designation of MED13L as a gene and its link to intellectual disability (ID) and dextro-looped transposition of great arteries in 2003, we previously described a recognizable syndrome due to MED13L haploinsufficiency. Subsequent reports of 22 further patients diagnosed by
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