نتایج جستجو برای: congenital congenital abnormalities vena cava

تعداد نتایج: 222405  

Journal: :Chest 1991
P J Giannoccaro J F Marquis K L Chan V Walley R J Chambers

plasmose generalisse avec localisation laryngee et endocaroite. An acute aortic dissection with rupture in the descending aorta led to suffusion of blood into the soft tissue of the neck with sufficient pressure to cause not only superior vena cava obstruction, but also trachea! obstruction. RA = right atrium; LA = left atrium; PA = pulmonary artery; Th = thrombus. Airtic dissection results fro...

2015
Tolga Atilla Sagban Rüdiger E Scharf Markus U Wagenhäuser Alexander Oberhuber Hubert Schelzig Klaus Grabitz Mansur Duran

BACKGROUND Congenital absence of the inferior vena cava (AIVC) is a rare malformation which may be associated with an increased risk for deep vein thrombosis (DVT). However, the role of thrombophilia in AIVC and DVT is unknown. METHODS Between 1982 and 2013 41 patients (12 female, 29 male, mean age 28 S.D. 11 years) were detected at the University of Düsseldorf, Germany, with AIVC. Based on m...

Journal: :Journal of Korean Medical Science 1993
Y. Park G. Gong G. Choe E. Yu K. S. Kim I. Lee

Jarcho-Levin syndrome (JLS) is a condition manifested by malformations of vertebral bodes and related ribs. There are two major subtypes spondylocostal dysostosis and spondylothoracic dysostosis, with different survival rates, associated malformations, and inheritance patterns. We have experienced an autopsy case of a premature female fetus with multiple congenital anomalies. She was 30 weeks o...

Journal: :iranian journal of radiology 0
fatmagul basarslan fesu~t}eov ogdygmoe rmws avesoecl ]o{vmvsm ynagu u{togn}eoocyoema}w{wsfa kemal university, turkey +90-3262291000/2827, [email protected]; fesu~t}eov ogdygmoe rmws

the ribs are essential structures of the osseous thorax that provide certain significant information and aid interpretation of radiologic images in daily routine practice. intrathoracic rib is a rare congenital anomaly that is usually discovered incidentally, but may cause in vain interventions in case of being unaware. we herein report an intrathoracic rib in a girl whose chest x-ray was stran...

Journal: :the journal of tehran university heart center 0
arash gholoobi atherosclerosis prevention research center, imam reza hospital, mashhad university of medical sciences, mashhad, iran. mohammad vojdanparast cardiovascular research center, mashhad university of medical sciences, mashhad, iran.

large intercoronary communications in the absence of obstructive coronary artery disease constitute a very rare coronary artery anomaly in which there is a readily visible connection between the 2 coronary arteries with a unidirectional or bidirectional blood flow; consequently, this anomaly may be misinterpreted as a functioning collateral vessel, indicative of an unrecognized proximal coronar...

Journal: :iranian journal of immunology 0
mohamed osama hegazi department of medicine, al adan hospital mohamed mourou department of medicine, al adan hospital omar ahmed hassanien department of radiology, yaco-al adan center, kuwait

0

Journal: :the journal of tehran university heart center 0
mohammad yousef aarabi moghaddam shaheed rajaei cardiovascular medical and research center, iran university of medical sciences, tehr hojatollah mortezaian shaheed rajaei cardiovascular medical and research center, iran university of medical sciences, tehr seyed reza miri shaheed rajaei cardiovascular medical and research center, iran university of medical sciences, tehr

cornelia de lange syndrome (cdls) is a rare syndrome characterized by multiple congenital anomalies, mental retardation, characteristic facial appearance, developmental delay, skeletal malformation, hirsutism, and various cardiac and ophthalmological problems. the diagnosis of this syndrome is clinical. the patient of the present case report was the second case of cdls from iran ; only a few ca...

Journal: :Cardiovascular Ultrasound 2008
Sandeep K Goyal Sujeeth R Punnam Gita Verma Frederick L Ruberg

Persistent left superior vena cava is rare but important congenital vascular anomaly. It results when the left superior cardinal vein caudal to the innominate vein fails to regress. It is most commonly observed in isolation but can be associated with other cardiovascular abnormalities including atrial septal defect, bicuspid aortic valve, coarctation of aorta, coronary sinus ostial atresia, and...

Journal: :Journal of medical genetics 1981
S Mantagos J W McReynolds M R Seashore W R Breg

Two unrelated newborn infants with multiple malformations were found to have complete trisomy 9 in all cells examined. In both, the phenotype was similar, consisting of characteristic facial appearance (microphthalmia, bulbous nose, micrognathia, cleft palate, low set ears), skeletal abnormalities (dislocated joints, flexion contractures of the fingers), cardiovascular malformations (persistent...

2010
Hamid Amoozgar Khobiar Zare Gholamhossein Ajami Mohammad Borzoee Saeed Abtahi

OBJECTIVE Paucity of data exists between mean right atrial pressure (RAP) and inferior vena cava (IVC) size and collapsibility in pediatric patients with congenital heart disease. METHODS In a prospective study, fifty consecutive pediatric patients with different congenital heart diseases who had right side cardiac catheterization were studied, comparing right atrial pressure with simultaneou...

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