Stress, coping, protective factors, and quality of life in parents of infants with CHD: associations with state anxiety [0.03%]
先天性心脏病婴儿父母的压力、应对方式、保护因素和生活质量与状态焦虑的相关性研究
Jessica Bainton,Felicia L Trachtenberg,D&#x;Andrea Freemon et al.
Jessica Bainton et al.
Introduction: The Family Adaptation study, ancillary to the Single Ventricle Reconstruction Trial, examined the prevalence of anxiety and its associations with stress, psychosocial factors, and quality of life measures in...
Leadless pacing in pre-adolescent patients weighing 30kg or less: case report and systematic review [0.03%]
无导线起搏器在体重30千克或以下的学龄前患者中的应用：病例报告和系统性回顾
Pipin Kojodjojo,Jeremy Chow
Pipin Kojodjojo
Transvenous and epicardial pacing in children carries significant risks of lead failure and infection. Leadless pacing is an alternative with lower risks of infection, lead failure, and longer battery longevity. A retrievable leadless pacem...
Favourable outcome of a neonate with vein of Galen malformation with concurrent right superior vena cava draining into the left atrium [0.03%]
合并右上腔静脉连接左心房的动静脉畸形胎儿出生后预后良好病例报道
Nabil Alhayek,Andrew Cave,Arshid Mir
Nabil Alhayek
We present a neonate with a large vein of Galen malformation and an unusual drainage of the large vein returning blood from the upper half of the body into the right atrium (superior vena cava) into the left atrium. Remarkably, the infant s...
Scimitar syndrome and single ventricle physiology: evolving strategies and the role of bridge-to-transplant therapy [0.03%]
弯刀综合征和单心室生理：演进策略与姑息治疗的作用
Alee Nicole Pettit,Lindsay Nitsche,Nikia Toomey et al.
Alee Nicole Pettit et al.
Scimitar syndrome is a rare CHD involving anomalous pulmonary venous drainage and lung hypoplasia. Severe cases complicate single ventricle palliation, prompting a shift to transplantation. Our case series highlights suboptimal outcomes des...
Bilateral absence of the superior vena cava in asymptomatic paediatric case [0.03%]
无症状儿童双侧上腔静脉缺如症案例分析
Ufuk İlker Sayıcı,Gokce Hasibe Cınar
Ufuk İlker Sayıcı
Variations in venous circulation can affect either the superior or inferior vena cava, with diagnoses often being incidental and presenting with highly variable symptoms. This rare case discusses the detection and investigation of bilateral...
Late diagnosis of Jervell and Lange-Nielsen syndrome in two sisters with homozygous KCNQ1 mutation [0.03%]
两个KCNQ1纯合突变Jervell和Lange-Nielsen综合征患者的确诊延迟
Peruze Kocaekiz,Onur Tokgun,Samet Yilmaz
Peruze Kocaekiz
Jervell and Lange-Nielsen syndrome is a rare inherited disorder characterised by sensorineural hearing loss and a prolonged corrected QT interval, predisposing to malignant arrhythmias. We describe two adult sisters diagnosed after recurren...
A novel homozygous PPP1R13L frameshift variant in a child with syndromic dilated cardiomyopathy and fatal arrhythmia [0.03%]
小儿致死性心律失常扩张型心肌病综合征中PPP1R13L错义变异的遗传咨询
Hakan Kurt,Zulal Ulger,Ertürk Levent et al.
Hakan Kurt et al.
Background: Dilated cardiomyopathy is a rare but severe myocardial disease in the paediatric population, often leading to heart failure, heart transplantation, or sudden cardiac death. Genetic factors are a major contribu...
Right ventricular function after repair of tetralogy of Fallot: an echocardiographic and clinical evaluation [0.03%]
法洛四联症矫正术后右心功能的超声及临床评价
Onur Benli,Mehmet Sah Topcuoglu,Mete Kasap
Onur Benli
Background: Right ventricular dysfunction is a major determinant of long-term outcomes after tetralogy of Fallot repair, particularly in the presence of chronic pulmonary regurgitation. Strain analysis may detect early ri...
Unexpected sudden cardiac arrest due to ventricular fibrillation in a 7-year-old boy with Duchenne muscular dystrophy [0.03%]
Duchenne肌营养不良7岁男孩意外发生室颤型心脏骤停
Christiane Mhanna,Shannon Nees,Takeshi Tsuda
Christiane Mhanna
A previously asymptomatic 7-year-old boy with Duchenne muscular dystrophy unexpectedly developed sudden cardiac arrest with no preceding illness. An automated external defibrillator confirmed the presence of ventricular fibrillation. Cardia...
Turner syndrome and acute type A aortic dissection: a national inpatient analysis of risk and outcomes [0.03%]
特纳综合征与急性A型主动脉夹层：风险和结局的全国住院患者分析
Yesh Datar,Avni Madhani,Kanhua Yin
Yesh Datar
Background: Although acute type A aortic dissection (ATAAD) is a recognised complication of Turner syndrome, population-level data describing its prevalence and outcomes remain limited. ...