Pentalogy of Cantrell: the complete spectrum.
نویسندگان
چکیده
To cite: Martins CF, Serras I, Santos AV, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2014-207556 DESCRIPTION A healthy 25-year-old primigravida, without a history of teratogenic exposition, presented to our hospital with a first trimester routine ultrasonographic examination showing two major fetal defects: gastrosquisis (figure 1 and video 1) and ectopia cordis (video 2). At 16 weeks of gestation a detailed ultrasound confirmed the suspected abnormalities together with sternal and diaphragm defects, and pentalogy of Cantrell was suspected. An amniocentesis and termination of the pregnancy were considered and
منابع مشابه
امفالوسل و قلب بیرون از قفسه سینه درنوزاد با Pentalogy of Cantrell
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 ...
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The pentalogy of Cantrell, a rare syndrome, consists of the defects in the anterior diaphragm, diaphragmatic pericardium, lower sternum and supraumbilical abdominal wall, along with congenital cardiac abnormalities. Till date, only few patients with full spectrum of this syndrome have been reported with only 2 cases showing associated exencephaly and spinal dysraphism. We report extremely rare ...
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BACKGROUND Pentalogy of Cantrell is a rare malformation syndrome consisting of a specific combination of ventral midline defects, uncommonly found to be associated with other anomalies. CASE We report a case of complete Pentalogy of Cantrell with craniorachischisis diagnosed in-utero at 19 weeks of gestation through antenatal ultrasonography. Fetal autopsy following termination of the pregnan...
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ورودعنوان ژورنال:
- BMJ case reports
دوره 2014 شماره
صفحات -
تاریخ انتشار 2014