Cardiovascular malformations and oesophageal atresia.

نویسندگان

  • T J David
  • S E O'Callaghan
چکیده

compared with 40 out of I56 patients (25.6%) who had oesophageal atresia with no other malformations. Persistent ductus arteriosus was the commonest lesion, followed by ventricular septal defect, secundum atrial septal defect, right-sided aortic arch, dextrocardia, anomalous right subclavian artery, and defects of the atrioventricular valves. Patients with cardiovascular malformations had a lower birthweight, a shorter gestation, and were more likely to have an abnormally low fetal growth rate. A right-sided aortic arch or an anomalous right subclavian artery in patients with oesophageal atresia should suggest the possibility of thymic orparathyroid hypoplasia or agenesis. Now that oesophageal atresia itself can be corrected, the associated cardiovascular malformations are of increasing importance.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Oesophageal atresia and associated anomalies.

Of 253 infants with oesophageal atresia treated over an eight year period, 122 (48%) had a total of 213 other anomalies. Most commonly affected were the cardiovascular (61 cases, 29%), anorectal (30 cases, 14%), and genitourinary (29 cases, 14%) systems. The VATER (or VACTERL) association was present in 10% of cases, but occurred more often in patients who had oesophageal atresia without an ass...

متن کامل

Oesophageal atresia, VACTERL association: Fanconi's anaemia related spectrum of anomalies.

Oesophageal atresia usually occurs without any genetic background. Three cases associated with Fanconi's anaemia are reported. One neonate had growth retardation and numerous malformations including oesophageal atresia and four other components of the VACTERL association. In the two others, oesophageal atresia was isolated. In patients with such malformations an early diagnosis of Fanconi's ana...

متن کامل

Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology.

Oesophageal atresia and/or tracheo-oesophageal fistula are relatively common malformations occurring in approximately 1 in 3500 births. In around half of the cases (syndromic oesophageal atresia), there are associated anomalies, with cardiac malformations being the most common. In the remainder (non-syndromic cases), oesophageal atresia/tracheo-oesophageal fistula occur in isolation. Data from ...

متن کامل

Oesophageal atresia, tracheo-oesophageal fistula and the VACTERL association: review of genetics and epidemiology. Charles Shaw-Smith Department of Medical Genetics, Addenbrooke’s Hospital, Cambridge CB2 2QQ, Address for correspondence:

Oesophageal atresia and/or tracheo-oesophageal fistula are common malformations occurring in approximately 1 in 3500 births. In around half of cases (syndromic oesophageal atresia), there are other associated anomalies, with cardiac malformations being the most common. These may occur as part of the VACTERL association (OMIM 192350). In the remainder of cases, oesophageal atresia/tracheo-oesoph...

متن کامل

Anorectal Malformation Associated with Small and Large Bowel Atresias: A Rare Association

Anorectal malformation (ARM) is one of frequent neonatal surgical problem managed in pediatric surgical units. Gastrointestinal malformations are associated in approximately 5% cases of ARM. Some of the common associations are oesophageal atresia and trachea oesophageal fistula, duodenal atresia, hirschsprung`s disease, pouch colon and neuronal intestinal dysplasia [1]. Association of ARM with ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • British heart journal

دوره 36 6  شماره 

صفحات  -

تاریخ انتشار 1974