OMPHALOCELE

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Familial omphalocele.

An omphalocele is an extrusion of the intestine and other abdominal contents through the umbilical ring. The prevalence rate varies with the methods of ascertainment. McKeown et al,1 in Birmingham in 1941-1951, found a prevalence rate of 1 in 3,200 liveand stillbirths, and in 1982, in Northern Ireland, the figure was 1 in 2,000 liveand stillbirths.2 It is usually sporadic, and familial occurren...

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Gastroschisis and omphalocele.

The newborn who has an abdominal wall defect is one of the most dramatic presentations in medicine and offers many challenging problems to the pediatric surgeon. This article presents the basics of the two most common abdominal wall defectsdgastroschisis and omphaloceledincluding principles and options of prenatal, postnatal, and surgical management. Although textbooks group the two entities to...

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Bedside Repair of Omphalocele

An omphalocele is one of the developmental anomalies of the abdominal wall. Incidence is 1.5-3 case per 10000 births. The abdominal viscera are surrounded by the Wharton jelly, peritoneum and amnion and contained in a translucent sac. The sac protrudes in the midline, through the umbilicus. Omphalocele is associated with additional anomalies in about 50-70% of cases. After the birth, defect is ...

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Antenatal diagnosis of isolated omphalocele

The concern of obstetric and surgical teams is when diagnosis of omphalocele, the care of the newborn and the prognosis of the malformation, mainly linked to the existence of associated malformations or chromosomal abnormalities. In our case of isolated omphalocele, the overall prognosis was good.

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Omphalocele with Intra Abdominal Anomalies

Abdominal wall defects are associated with other intra-abdominal anomalies. We report two neonates with omphalocele associated with intra-abdominal anomalies. One neonate had multicystic kidney. Other neonate had duplication cyst of ileum which was missed during initial closure in neonatal life.

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ژورنال

عنوان ژورنال: JOURNAL OBGIN EMAS

سال: 2019

ISSN: 2579-8324,2579-8413

DOI: 10.25077/aoj.2.1.62-66.2018