نتایج جستجو برای: congenital anomaly

تعداد نتایج: 151428  

Journal: :European journal of echocardiography : the journal of the Working Group on Echocardiography of the European Society of Cardiology 2008
Sridevi R Pitta Ashok Kondur Luis Afonso

Quadricuspid aortic valve is a rare congenital anomaly. It may present as an isolated anomaly but is occasionally associated with aortic regurgitation. Sinus of Valsalva aneurysm (SVA) is also an infrequent congenital anomaly, typically associated with tricuspid aortic valves. There are only a few reported cases of SVA (ruptured) associated with quadricuspid aortic valves in the literature. We ...

Journal: :The American journal of cardiology 1953
J F GOODWIN A WYNN R E STEINER

Ebstein's anomaly of the tricuspid valve is a rare lesion comprising less than 1% of patients with congenital heart disease. Among congenital heart lesions, Ebstein's anomaly is one of the most diverse in presentation, severity, and management. In its most severe form, it is also one of the most lethal. In this article we present a case of a patient who developed cardiac symptoms in adulthood. ...

A. Fazel A. Niazi A. Omidi, M. Gharavian N. Sharifi

Bilateral femoral agenesis is a rare anomaly.  To the best of our knowledge, only three cases of simple congenital anomaly and three cases associated with femoral facial syndrome have been reported.  Here, we describe a simple form of bilateral femoral agenesis observed in one of the 2 dead fetuses delivered after termination of a 24-week twin pregnancy of a normal mother.  Post-mortem x-ray ex...

ژورنال: یافته 2012
طائی, نادره , فرجی گودرزی, مژگان, فیروزی, مجید ,

Background : Pentalogy of Cantrell is a very rare congenital anomaly which is diagnosed with severe thoracoabdominal defect, omphalocele, lower sternal defect, anterior diaphragmatic defect anterior pericardial defect and ectopia cordis.Pathogenesis is unknown, mesodermal developmental defects in 14-18 days after conception maybe responsible . Case Report: The case is newborn with omphalocele ...

2008
Hee Jung Suh Wan Tae Kim Mi Young Kim Yun Ku Cho

The absence of the inferior vena cava is an uncommon congenital anomaly that has recently been identified as an important risk factor contributing to the development of deep venous thrombosis. Congenital agenesis of the right hepatic lobe is a rare anomaly which is found incidentally in radiologic examinations. We present a case of a congenital absence of the infrarenal inferior vena cava, comb...

Hossein Nough, Zahra Ansari

Congenital absence of left circumflex artery is a rare congenital anomaly of the coronary arteries. The prevalence of the anomaly in different studies ranges from 0.6% to 1.3%. Of these, 80% are benign and asymptomatic and 20% are clinically important. We report a 56-year-old man presented with acute resting chest pain who was diagnosed as having acute anterolateral infarction accompanied by el...

Journal: :Indian pediatrics 1994
R Khadagawat R Teckchandani P Garg A Arya B Choudhary

The importance of identifying this anomaly is that it is associated with other congenital malformations in over 20% of cases, most commonly being associated with cardiovascular anomalies and congenital dislocation of hip. Of the 44 infants with this syndrome, Pape and Pickering found 27 to have major anomaly of skeletal, genitourinary, respiratory and cardiovascular systems. The disorder most c...

Habibollah Saadat, Mohamadreza Motamedi, Naser Alihojati,

​Congenital anomalies of the coronary arteries have been a known subject  since the advent of cardiac angiography, and has been a subject of special interest by both cardiologists and cardiac surgeons,  We have tried in this article to present a case of anomalous origin of LAD from RCA (RMT) in a 55 year old lady (Mrs. B.J.) and to completely dis­cuss this subject. It's worthmentioning that thi...

Journal: :مجله دانشکده پزشکی دانشگاه علوم پزشکی تهران 0
محمود فرزان farzan m حسین عطائی فشتمی attaei h

cleft hand deformity is a rare congenital anomaly of the hand with an incidence rate about 1/90,000. it has two clinical types typical and atypical. in this paper we are representing ten cases of this anomaly admitted during seven years from 1992 in emam khomeini hospital. some of the patients especially those with typical cleft hand deformity achieved good functional results after surgical cor...

Journal: :iranian journal of medical sciences 0
a. omidi n. sharifi a. fazel a. niazi m. gharavian

bilateral femoral agenesis is a rare anomaly.  to the best of our knowledge, only three cases of simple congenital anomaly and three cases associated with femoral facial syndrome have been reported.  here, we describe a simple form of bilateral femoral agenesis observed in one of the 2 dead fetuses delivered after termination of a 24-week twin pregnancy of a normal mother.  post-mortem x-ray ex...

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