نتایج جستجو برای: congenital heart malformation

تعداد نتایج: 493580  

Journal: :Folia morphologica 2004
Metin Demircin Murat Guvener O Faruk Dogan Selcuk Tunali M Mustafa Aldur H Hamdi Celik

The authors report a case of double-orifice mitral valve (DOMV) which showed mitral stenosis and mild insufficiency. An associated anomaly was secundum atrial septal defect. DOMV is an unusual congenital heart defect. The occurrence of this anomaly with or without secundum atrial septal defect is very rare. More often it is associated with other congenital malformations arising from atrioventri...

Journal: :Fetal diagnosis and therapy 2011
Paweł Sadłecki Michał Krekora Grzegorz Krasomski Małgorzata Walentowicz-Sadłecka Marek Grabiec Jacek Moll Maria Respondek-Liberska

Ectopia cordis (EC) is a rare malformation due to failure of maturation of the midline mesodermal components of the chest and abdomen. It can be defined as a complete or partial displacement of the heart outside the thoracic cavity. It comprises 0.1% of congenital heart diseases. Common cardiac anomalies associated with EC are ventricular septal defect, atrial septal defect, and tetralogy of Fa...

Journal: :Anesthesiology 2010
Kha M Tran Mark P Johnson Gracie M Almeida-Chen Alan Jay Schwartz

A 19-WEEK PARTURIENT presented with a fetus with a lung mass. Magnetic resonance imaging (panel A) demonstrated a congenital cystic adenomatous malformation (CCAM) occupying the right chest causing mediastinal shift, cardiac compression (H heart), and displacement of the hemidiaphragm (arrow). Both lungs were compressed. Hydrops fetalis was present (A fetal ascites; B bowel; L liver). Echocardi...

2013
Mehmet Demir

Bicuspid aortic valve (BAV) represents the most common cardiac congenital malformation in the adult age, with strong male predominance. It may occur in isolation, or in association with other congenital heart diseases. The BAV is seen in 1% to 2% of the population and may be complicated by aortic stenosis or aortic insufficiency and infective endocarditis. It may be associated with abnormalitie...

Journal: :Circulation 1998
D W Benson A Sharkey D Fatkin P Lang C T Basson B McDonough A W Strauss J G Seidman C E Seidman

BACKGROUND Secundum atrial septal defect (ASD) is a common congenital heart malformation that occurs as an isolated anomaly in 10% of individuals with congenital heart disease. Although some embryological pathways have been elucidated, the molecular etiologies of ASD are not fully understood. Most cases of ASD are isolated, but some individuals with ASD have a family history of this defect or o...

2011
Pedro R Coutinho José G Cecatti Fernanda G Surita Maria L Costa Sirlei S Morais

OBJECTIVE To identify perinatal outcomes associated with low birth weight (LBW). METHODS A retrospective cohort study in a tertiary maternity hospital. Analysis of the database on 43,499 liveborn infants delivered between 1986 and 2004 with low (n = 6,477) and normal (n = 37,467) birth weight. Outcomes associated with LBW were identified through crude and adjusted risk ratio (RR) and 95%CI wi...

Akhavan Karbasi S Fallah R Golestan M

Background: Congenital malformation (CM) is the major health problems in childhood because treatment and rehabilitation of children with CM is costly and complete recovery is usually impossible. For most of single primary defect the etiology is unknown. The aim of this study was to determine frequency of CM and its association with maternal age. Materials and Methods: This descriptive-observati...

Journal: :International journal of pediatric otorhinolaryngology 2005
Neeraj N Mathur Indu Rana Rajendra Bothra Rajiv Dhawan Geeta Kathuria Tapaswini Pradhan

Bleomycin is an established antineoplastic drug, but recently some attempts were made to inject it locally as a sclerosing agent in cases of congenital lymphatic malformations. We present the outcome of this treatment modality tried on 10 paediatric cases of whom 9 had such malformation in the cervical region and one in the parotid region. Seven of these cases had congenital lymphatic malformat...

2014
Derya Arslan Derya Cimen Osman Guvenc Bulent Oran

Anomalous systemic venous return (AVSR) may sometimes present as pathologic entities itself, or associated with other congenital heart defects. The presence of AVSR may require significant changes in surgical technique during the repair of congenital heart defects. The aim of our study was to assess the prevalence of anomalous systemic venous return and to determine the congenital heart anomali...

Journal: :Human reproduction 2004
U Ulrich J Schrickel C Dorn O Richter T Lewalter B Lüderitz K Rhiem

We report on the association of Mayer-von Rokitansky-Küster-Hauser syndrome (MRKHS) with a unique form of Holt-Oram syndrome (HOS) with an aorto-pulmonary window. A 24-year-old Turkish woman was referred to our hospital because of primary amenorrhoea. Both her vagina and uterus were absent, and the diagnosis of MRKHS was established. Laparoscopic creation of a neovagina by the modified Vecchiet...

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