A rare case of cardiac anomaly: prenatally diagnosed ectopia cordis
نویسندگان
چکیده
منابع مشابه
A rare case of cardiac anomaly: prenatally diagnosed ectopia cordis.
Ectopia cordis is a rare congenital malformation in which the heart is located partially or totally outside the thoracic cavity. The estimated prevalence of ectopia cordis is 5.5-7.9 per million births and it comprises 0.1% of congenital heart diseases. Ectopia cordis is associated with other congenital heart diseases and various tissue and organ disorders. Common cardiac anomalies associated w...
متن کاملPartial Ectopia Cordis: A Case Report
Background: One-third of all major congenital anomalies are Congenital heart disease (CHD) and Reported CHD prevalence increased over time and in Asian countries is more than western countries. Ectopia cordis (EC) is a rare congenital anomaly with an estimated incidence of 1:100 000 live births in developed countries. EC is characterized by abnormal heart placement outside the thorax, mostly on...
متن کامل[Ectopia cordis and cardiac anomalies].
Ectopia cordis is a rare disease that occurs in 5.5 to 7.9 per million live births. Only 267 cases had been reported as of 2001, most (95%) associated with other cardiac anomalies. We studied the cardiac malformations associated in 6 patients with ectopia cordis. Depending on where the defect was located, the cases of ectopia were classified into four groups: cervical, thoracic, thoraco-abdomin...
متن کاملPrenatally evolving ectopia cordis with successful surgical treatment.
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...
متن کاملEctopia Cordis anesthetic considerations a case report
Introduction: Ectopia cordis is a rare congenital defect and a true neonatal surgical emergency, with an occurrence of 5.5 to 7.9 cases per million live births [1]. This impressive malformation develops due to failure of maturation of the midline mesodermal components of the chest and abdomen [2]. The disorder is classified into five anatomical types including cervical, cervicothoracic, thoraci...
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ژورنال
عنوان ژورنال: Türk Pediatri Arşivi
سال: 2015
ISSN: 1306-0015,1308-6278
DOI: 10.5152/tpa.2015.927