Developmental considerations with regard to so-called absence of the leaflets of the arterial valves.

Abstract:

BACKGROUND:Absent arterial valve leaflets are rare anomalies. On the basis of our understanding of the normal development of the arterial valves, we draw inferences that might offer clues to their morphogenesis. METHODS:We describe the findings from four human fetal autopsies with so-called "absent" arterial valvar leaflets. We then make inferences relative to these finding on the basis of our current understanding of normal development, the latter obtained by analysis of episcopic data sets from a large series of mouse embryos. RESULTS:The fetuses had died between 12 and 15 weeks of gestation. In two cases, we found absence of the leaflets of the pulmonary valve, with patency of the arterial duct, but otherwise normal hearts. In a third case, there was absence of the leaflets of both arterial valves, along with a perimembranous ventricular septal defect and a "window-type" arterial duct. This fetus had a completely muscular subaortic infundibulum. The last fetus had a pulmonary dominant common arterial trunk, with absence of the truncal valvar leaflets, but again with a muscular subtruncal infundibulum. Findings from the analysis of the mouse embryos reveal that the arterial valvar leaflets are formed from the distal outflow cushions, but that the cushions have a separate function in septating the arterial roots and the proximal outflow tracts. CONCLUSIONS:When interpreting the fetal findings in the light of development, we conclude that there had been normal fusion of the major outflow cushions, but failure in excavation of their peripheral margins in three of the cases. In the fourth case, however, the cushions had not only failed to excavate but had also failed to separate the arterial roots.

journal_name

Cardiol Young

journal_title

Cardiology in the young

authors

Tretter JT,Steffensen T,Westover T,Anderson RH,Spicer DE

doi

10.1017/S1047951116000524

subject

Has Abstract

pub_date

2017-03-01 00:00:00

pages

302-311

issue

2

eissn

1047-9511

issn

1467-1107

pii

S1047951116000524

journal_volume

27

pub_type

杂志文章
  • "Shunt index" can be used to predict clinically significant patent ductus arteriosus in premature neonates in early post-natal life.

    abstract:BACKGROUND:This study aimed to examine the differences between arterial and inferior caval vein oxygen saturation, fractional oxygen extraction, and the shunt index, which were calculated in the diagnosis of patent ductus arteriosus. METHODS:Twenty-seven preterm infants were included in this study and were divided int...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951113000772

    authors: Yapakçı E,Ecevit A,Törer B,Ince DA,Gökdemir M,Gülcan H,Tarcan A

    更新日期:2014-08-01 00:00:00

  • Unique foetal diagnosis of aorto-pulmonary collaterals in right atrial isomerism.

    abstract::Right atrial isomerism is associated with complex cardiac malformations, particularly single-ventricle lesions; right atrial isomerism is rarely associated with aorto-pulmonary collateral arteries. We report a foetal diagnosis of right atrial isomerism, with an unbalanced atrioventricular septal defect, pulmonary sten...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120003649

    authors: Mawad W,Dutil N,Thakur V

    更新日期:2020-11-26 00:00:00

  • Holt-Oram syndrome: novel TBX5 mutation and associated anomalous right coronary artery.

    abstract::The Holt-Oram syndrome was confirmed in an asymptomatic 36-year-old man by a novel TBX5-gene mutation (exon 8 acceptor splicing site, c.663-1G greater than A). Computed tomography showed an atrial septal defect and an anomalous right coronary artery crossing between the aorta and pulmonary arteries. Surgery corrected ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951111000072

    authors: Vianna CB,Miura N,Pereira AC,Jatene MB

    更新日期:2011-06-01 00:00:00

  • Cardiac strain findings in children with latent rheumatic heart disease detected by echocardiographic screening.

    abstract:BACKGROUND:Identification of patients with latent rheumatic heart disease by echocardiography presents a unique opportunity to prevent disease progression. Myocardial strain is a more sensitive indicator of cardiac performance than traditional measures of systolic function. OBJECTIVE:The objective of this study was to...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951116002778

    authors: Beaton A,Richards H,Ploutz M,Gaur L,Aliku T,Lwabi P,Ensing G,Sable C

    更新日期:2017-08-01 00:00:00

  • Physical activity and obesity in children with congenital cardiac disease.

    abstract:BACKGROUND:Children with congenital cardiac disease experience challenges in developing healthy patterns of physical activity due to decreased exercise capacity and parental fear and confusion about what is permissible. The purpose of this study was to describe physical activity habits in children 10-14 years of age wi...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951111000540

    authors: Ray TD,Green A,Henry K

    更新日期:2011-12-01 00:00:00

  • Duration and dispersion of the P wave after the Senning operation.

    abstract::We studied the duration and dispersion of the P wave in patients after a Senning operation, assessing its value in detecting the risk of atrial tachycardias.We measured the duration and dispersion of the wave in surface 12 lead electrocardiograms obtained from 18 patients with sinus rhythm, having a mean age of 12.8 y...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951109991892

    authors: Ozyilmaz I,Eroğlu AG,Güzeltaş A,Oztunç F,Saltik L,Ozdil M,Bariş S

    更新日期:2009-12-01 00:00:00

  • The impact of the severity of disease and social disadvantage on quality of life in families with congenital cardiac disease.

    abstract:OBJECTIVE:Increasing rates of survival have raised the question of medical and psychosocial factors contributing to quality of life of patients with congenital cardiac disease. We investigated the impact of the severity of disease, and social disadvantage, on the quality of life of patients and their primary caregivers...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951105002118

    authors: Goldbeck L,Melches J

    更新日期:2006-02-01 00:00:00

  • Transcatheter closure of a multiperforated atrial septal defect extending from the oval fossa to the mouth of the inferior caval vein.

    abstract::We report a novel technique using an Amplatzer atrial septal occluder to close a defect located in the inferior-posterior portion of the interatrial septum that extended into the mouth of the inferior caval vein. Because of the close relation of the defect to the inferior caval vein, the right atrial disc was opened i...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951103000386

    authors: Peuster M,Reckers J,Fink C

    更新日期:2003-04-01 00:00:00

  • How implantable cardioverter-defibrillators work and simple programming.

    abstract::Following the sudden death of a friend in 1966, Dr Michel Mirowski began pioneering work on the first implantable cardioverter-defibrillator. By 1969 he had developed an experimental model and performed the first transvenous defibrillation. In 1970 he reported on the use of a "standby automatic defibrillator" that was...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,评审

    doi:10.1017/S1047951116002353

    authors: Bryant RM

    更新日期:2017-01-01 00:00:00

  • Outcome of ligation of the persistently patent arterial duct in neonates as performed by an outreach surgical team.

    abstract:AIM:Our aim was to review the outcome of ligation of the persistently patent arterial duct in neonates as performed outside a paediatric cardiothoracic centre by an outreach surgical team. METHODS:A retrospective observational study of all ligations of the persistently patent arterial duct performed in Cambridge betwe...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951107000741

    authors: Sivakumar S,Lee L,Tillett A,Wells F,Dunning J,Kelsall AW

    更新日期:2007-10-01 00:00:00

  • Endocarditis of a congenital coronary fistula in a child.

    abstract::Endocarditis of congenital coronary fistulas in the cardiac chambers is rare, especially in the paediatric age group. We describe the case of a 9-year-old boy with a fistula from the dilated right coronary artery to the junction of the superior caval vein to the right atrium, complicated by endocarditis. Treatment con...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951117001846

    authors: Krasemann T,van Beynum IM,Frohn-Mulder IME,Dalinghaus M

    更新日期:2018-02-01 00:00:00

  • An epicardial cyst in a child.

    abstract::An 8-year-old girl, without any previous medical history, presented with a first short syncope. Physical examination was unremarkable. Transthoracic echocardiography revealed a thin-walled, echo-free cystic structure adjacent to the posterior wall of the left ventricle, and compressing it moderately. Other echocardiog...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951101001056

    authors: Debus V,Krasemann T,Semik M

    更新日期:2001-11-01 00:00:00

  • Outcome for patients with isolated atrial septal defects in the oval fossa diagnosed in infancy.

    abstract:OBJECTIVE:Our aim was to investigate the change in diameter of holes within the oval fossa, and the role of aneurismal formation in reducing the size of the hole, in patients diagnosed during infancy with isolated defects in the floor of the fossa. PATIENTS:In a retrospective study, we included 100 patients diagnosed ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951107001692

    authors: Demir T,Oztunç F,Eroğlu AG,Saltik L,Ahunbay G,Kutluğ S,Güzeltaş A,Altun G

    更新日期:2008-02-01 00:00:00

  • Acquired ventricular septal aneurysm in a patient with pulmonary atresia with intact ventricular septum.

    abstract::Myocardial ischaemia and infarction in pulmonary atresia and intact ventricular septum with right ventricular-dependent coronary circulation is a well-established complication. We report an interesting case of an acquired aneurysm in the ventricular septum in a patient who underwent staged palliation. ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951111001120

    authors: Patel AR,Farrell P,Harris M,Gaynor JW,Gillespie MJ

    更新日期:2012-04-01 00:00:00

  • Anomalous origin of a single coronary artery from the pulmonary artery associated with patent ductus arteriosus.

    abstract::We report an unusual case of a 12-month-old boy diagnosed with anomalous origin of a single coronary artery from the pulmonary artery associated with patent ductus arteriosus. The patient survival was attributed to left-to-right shunt (patent ductus arteriosus) allowing for appropriate myocardial perfusion. Successful...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120001328

    authors: Hugues N,Dommerc C,Pretre R

    更新日期:2020-07-01 00:00:00

  • Coronary sinus stenosis: an underdiagnosed cause for paediatric exertional chest pain.

    abstract::Undiagnosed coronary sinus obstruction can be a source of paediatric exertional chest pain and death. We present a case series of three interesting children who developed only exertional angina from various degrees of coronary sinus stenosis or atresia. We discuss the diagnosis and management of each case and the pote...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120000918

    authors: Hegde SA,Moore J,Suarez WA

    更新日期:2020-06-01 00:00:00

  • Aortic elasticity and carotid intima-media thickness in children with mitral valve prolapse.

    abstract::Aim We aimed to study the dimensions, systolic and diastolic functions of the left ventricle; dimensions and elasticity of the aorta; and carotid intima-media thickness and flow-mediated dilatation of the brachial artery in mitral valve prolapse. METHODS:The study group consisted of 43 patients (mean age=13.3±3.9) an...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951117001950

    authors: Erolu E,Akalın F,Çetiner N,Şaylan Çevik B

    更新日期:2018-02-01 00:00:00

  • Is the burden of late hypertension and cardiovascular target organ damage in children and adolescents with coarctation of the aorta after early successful repair different to healthy controls?

    abstract:OBJECTIVE:Cardiovascular morbidity is high in patients with coarctation of aorta even after successful repair. This study aimed to assess the frequency of late hypertension and the relationship between ambulatory hypertension and cardiovascular target organ damage in children and adolescents after early and successful ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S104795112000205X

    authors: Ağbaş A,Gökalp S,Canpolat N,Çalışkan S,Öztunç F

    更新日期:2020-09-01 00:00:00

  • Sudden death in a patient with Noonan syndrome.

    abstract::We report here the case of a 27-year-old woman with Noonan syndrome presenting with ventricular fibrillation. After successful defibrillation, echocardiography revealed hypertrophic cardiomyopathy associated with left ventricular outflow tract obstruction. Normal echocardiographic cardiac structure and function were r...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951110001708

    authors: Aydin A,Yilmazer MS,Gurol T

    更新日期:2011-04-01 00:00:00

  • Irreversible coronary aneurysm presenting as acute coronary syndrome in a child with hypereosinophilic syndrome: a case report.

    abstract::Hypereosinophilic syndrome is defined as persistent eosinophilia in the blood for more than 6 months, without any identifiable cause and with end-organ involvement evidence. Cardiac manifestations of HES include heart failure due to restrictive cardiomyopathy, arrhythmia, intraventricular thrombosis, and coronary arte...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120004862

    authors: Tahouri T,Mahdavi M,Rezaei-Kalantari K,Shahzadi H

    更新日期:2021-01-25 00:00:00

  • Tetralogy of Fallot with unilateral absent pulmonary artery.

    abstract:BACKGROUND:Tetralogy of Fallot is a common congenital cardiac malformation. A rare subgroup includes unilateral absence of the pulmonary artery, either the left or the right main branch. The literature lacks an established treatment for these cases, and surgical options carry certain mortality and morbidity. PATIENTS ...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951112000911

    authors: Ugurlucan M,Arslan AH,Yildiz Y,Ay S,Besikci RT,Cicek S

    更新日期:2013-06-01 00:00:00

  • Dexmedetomidine utilisation and outcomes of children with trisomy 21 undergoing congenital heart disease surgery.

    abstract:INTRODUCTION:The diagnosis of trisomy 21 in children has been associated with failed extubation after CHD surgery. Dexmedetomidine may be a useful agent to improve postoperative outcomes in these patients, such as ventilator time, ICU length of stay, or hospital length of stay. MATERIALS AND METHODS:The Pediatric Heal...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951114001462

    authors: Moffett BS,Mossad EB,Tobias JD,Cabrera AG

    更新日期:2015-06-01 00:00:00

  • Individual and joint effects of genetic polymorphisms in microRNA-machinery genes on congenital heart disease susceptibility.

    abstract::Single-nucleotide polymorphisms in miRNA-machinery genes may alter the biogenesis of miRNAs affecting disease susceptibility. In this case-control study, we aimed to evaluate the impact of three single-nucleotide polymorphisms (DICER rs1057035, DROSHA rs10719, and XPO5 rs11077) and their combined effect in a genetic r...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951120004874

    authors: Borghini A,Vecoli C,Mercuri A,Turchi S,Andreassi MG

    更新日期:2021-01-11 00:00:00

  • Do toxic metals and trace elements have a role in the pathogenesis of conotruncal heart malformations?

    abstract:OBJECTIVE:The aim of the present study was to determine the role of toxic elements and trace elements in the pathogenesis of conotruncal heart defects by measuring their concentrations in the first meconium specimens of the affected newborns. METHODS:Concentrations of lead, cadmium, iron, zinc, and copper were measure...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951116000536

    authors: Kundak AA,Pektas A,Zenciroglu A,Ozdemir S,Barutcu UB,Orun UA,Okumus N

    更新日期:2017-03-01 00:00:00

  • Evaluation of cardiac autonomic function using heart rate variability in children with acute carbon monoxide poisoning.

    abstract::Introduction Carbon monoxide poisoning may cause myocardial toxicity and cardiac autonomic dysfunction, which may contribute to the development of life-threatening arrhythmias. We investigated the potential association between acute carbon monoxide exposure and cardiac autonomic function measured by heart rate variabi...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951117000944

    authors: Vural C,Dinleyici EC,Kosger P,Bolluk O,Kilic Z,Ucar B

    更新日期:2017-11-01 00:00:00

  • Preoperative identification of coronary arterial anatomy in complete transposition, and outcome after the arterial switch operation.

    abstract:BACKGROUND:Perceived correlation between the coronary arterial anatomy in patients with complete transposition, and the outcome of the arterial switch procedure, has made preoperative identification of their patterns standard practice. PURPOSE:Our purpose was to assess the accuracy of preoperative echocardiographic id...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951102000537

    authors: McMahon CJ,el Said HG,Feltes TF,Watrin CH,Hess BA,Fraser CD Jr

    更新日期:2002-05-01 00:00:00

  • Constriction of the ductus arteriosus, severe right ventricular hypertension, and a right ventricular aneurysm in a fetus after maternal use of a topical treatment for striae gravidarum.

    abstract::Fetal constriction of the ductus arteriosus is a complication of maternal non-steroidal anti-inflammatory drug use and polyphenol-rich food intake. It is unclear as to whether polyphenol-containing topical treatments have similar effects. We present a case of fetal constriction of the ductus arteriosus, severe right v...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951115001924

    authors: Hayes DA

    更新日期:2016-04-01 00:00:00

  • Spontaneous aortic thrombosis in neonates: a case report and review of literature.

    abstract::Neonatal aortic thrombosis is a rare occurrence but can be life-threatening. Most aortic thrombosis in neonates is related to umbilical artery catheters. A case of a neonate with a spontaneous aortic thrombosis is described here along with a comprehensive review of the literature for cases of neonatal aortic thrombosi...

    journal_title:Cardiology in the young

    pub_type: 杂志文章,评审

    doi:10.1017/S1047951119003093

    authors: Mulcaire-Jones JP,Bailly DK,Frank DU,Verma AR,Barney BJ,Siefkes HM

    更新日期:2020-01-01 00:00:00

  • Transcatheter closure of atrial septal defects within the oval fossa: medium-term results in children using the 'ASDOS'-technique.

    abstract:OBJECTIVES:The purpose of this study was to evaluate the safety and efficacy of the ASDOS-technique (Sulzer-Osypka GmbH, Germany) for transcatheter closure of atrial septal defects within the oval fossa. BACKGROUND:Although several attempts have been made to occlude defects within the oval fossa by transcatheter techn...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/s1047951100007125

    authors: Hausdorf G,Schneider M,Fink C,Neudorf U,Fischer G,Tynan M,Friedli B

    更新日期:1998-10-01 00:00:00

  • Atretic anomalous left subclavian artery as part of an unusual vascular ring.

    abstract::In this report, a unique case of a symptomatic vascular ring formed by right aortic arch, aberrant left subclavian artery, and left ligamentum arteriosus in which there is atresia of the proximal left subclavian artery is described. Imaging modalities were non-diagnostic and the patient was sent to surgery based on st...

    journal_title:Cardiology in the young

    pub_type: 杂志文章

    doi:10.1017/S1047951118001737

    authors: Powell SK,Patel JK,Ebenroth ES

    更新日期:2019-01-01 00:00:00