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omphalocele

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omphalocele /om·pha·lo·cele/ (om´fah-lo-sēl″) protrusion, at birth, of part of the intestine through a defect in the abdominal wall at the umbilicus.
om·phal·o·cele (m-fl-sl, mf-l-)
n.
Congenital herniation of viscera into the base of the umbilical cord. Also called exomphalos.

Omphalocele
A congenital hernia in which a small portion of the fetal abdominal contents, covered by a membrane sac, protrudes into the base of the umbilical cord.
Mentioned in: Prenatal Surgery

omphalocele
[om′fəlōsēl′]
Etymology: Gk, omphalos + kele, hernia
congenital herniation of intraabdominal viscera through a defect in the abdominal wall around the umbilicus. The defect is usually closed surgically soon after birth. Compare gastroschisis.

omphalocele [om´fah-lo-sēl″]
protrusion, at birth, of part of the intestine through a defect in the abdominal wall at the umbilicus; see also umbilical hernia.
A large omphalocele with structure and contents of the hernial sac. From Betz et al., 1994.

omphalocele
protrusion, at birth, of part of the intestine through a defect in the abdominal wall at the umbilicus.

omphalocele
Neonatology A congenital periumbilical defect in which loops of small intestine prolapse into a sac covered by peritoneum and amnion


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Extrarenal anomalies associated with horseshoe kidney include congenital heart defects (such as ventricular septal defect and coarctation), central nervous system disorders (such as hydrocephalus and meningomyelocele), and various other gastrointestinal anomalies (such as omphalocele, tracheoesophageal fistula, and duodenal stenosis).
There also were small but significant associations with anencephaly (based on 9 exposed neonates), craniosynostosis (based on 24 exposed neonates), and omphalocele (based on 11 exposed neonates).
2) There is a definite association of PMD with BWS, which is characterized by macrosomia, exomphalos, macroglossia, omphalocele, and internal visceromegaly in addition to placentomegaly and increased susceptibility to childhood tumors.
 
 
 
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