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Tetralogy of Fallot with pulmonary atresia and aortopulmonary window may mimic common arterial trunk
Publikováno v:
Cardiology in the Young. 32:410-414
Tetralogy of Fallot with pulmonary atresia is a group of congenital cardiac malformations, which is defined by the absence of luminal continuity between both ventricles and the pulmonary artery, and an interventricular communication. Pulmonary arteri
Publikováno v:
Cardiology in the Young. 32:398-404
Complete atrioventricular canal defect is a CHD associated with intra-cardiac shunting of blood, which can lead to irreversible changes in pulmonary vascular resistance and pulmonary artery hypertension if unrepaired. Patients with Trisomy 21 are at
Autor:
Shinichiro Yamashita, Daisuke Sugawara, Eishi Makita, Yuka Hirakubo, Kazuhito Nonaka, Misa Matsuura, Ko Ichihashi
Publikováno v:
Cardiology in the Young. 32:405-409
Background:Several studies have reported treatment options for patients with Kawasaki disease refractory to standard immunoglobulin therapy; however, no studies have reported low-dose immunoglobulin therapy for patients with a low risk of Kawasaki di
Publikováno v:
Cardiology in the Young. 32:244-251
The incidence of airway obstruction in patients with complex CHD other than vascular rings and absent pulmonary valve syndrome is unknown. We reviewed pre-operative CT and clinical data of children with conotruncal abnormalities to assess for airway
Publikováno v:
Cardiology in the Young. 32:266-269
Background:Anorexia nervosa has a prevalence of 0.5–3% in adolescents, placing this population at increased risk of cardiac anomalies including arrhythmias, pericardial effusion, and myocardial dysfunction. Our objective is to describe cardiovascul
Publikováno v:
Cardiology in the Young. 31:1193-1196
Extensive screening in a newborn with prenatal suspicion of VACTERL syndrome identified an anomalous origin of the left pulmonary artery from the descending aorta with an arterial duct and left aortic arch, and normal intra-cardiac anatomy. Other ana
Autor:
Haifa Abdul Latiff, Putri Yubbu, Nurul Adha Mohd Razif, Navin Kumar Devaraj, Husna Musa, Hasri Samion, Sivakumar Sivalingam
Publikováno v:
Cardiology in the Young. 32:374-382
Background:Vascular compression of the airway often complicates CHD management. This study evaluated the use of CT in determining cardiovascular causes, clinical manifestations, and outcome of tracheobronchial compression among children with CHD.Meth
Publikováno v:
Cardiology in the Young. 32:60-63
Isolated sub-pulmonary membrane is a rare condition, the origin of which has been debatable. Transcatheter treatment of pulmonary valve atresia with intact interventricular septum by radiofrequency perforation and balloon dilatation to restore bivent
Autor:
Sonia A. El-Saiedi, Reham Zeyada, Nadida A. Gohar, Dina A. Mehaney, Amira K. Embaby, Mohamed Abouelhoda, Zeinab Salah Seliem, Rania Kamal Darwish, Nesrine S. Elfeel, Alireza Haghighi
Publikováno v:
Cardiology in the Young. 32:295-300
Background:Paediatric cardiomyopathy is a progressive, often lethal disorder and the most common cause of heart failure in children. Despite its severe outcomes, the genetic aetiology is still poorly characterised. High-throughput sequencing offers a
Autor:
Damla Geçkalan Soysal, Rahmi Özdemir
Publikováno v:
Cardiology in the Young. 32:203-207
Background:Platelet indices are used to evaluate platelet activation and function which change in inflammatory diseases. We hypothesise that platelet indices such as plateletcrit, mean platelet volume, and platelet distribution width may be more usef