Gastroschisis vs omphelocele
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Gastroschisis vs omphelocele
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Gastroschisis |
omphelocele
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Incidence 1: 10,000 |
Incidence 2.5: 10,000 |
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M:F: 1:1 |
M:F: 1.5:1 |
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Ventral abdominal wall defect resulting from a lack of closure of the lateral body wall folds in the abdominal region resulting in protrusion of intestines and sometimes other organs through the defect lateral to the umbilicus usually on the right
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Ventral abdominal wall defect caused by failure of physiologically herniated loops of bowel to return to the abdominal cavity in the 10th week |
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It is developed earlier than the omphelocele 3rd to 4th week of gestation when lateral folds of embryonic disc l fail to fuse together |
Physiological umbilical herniation of intestinal loops develops at 6th week of intrauterine life and normally it start to return at 10th week of intrauterine life. In omphelocele intestinal loops fails to return so herniation persists |
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It is more occurs in young women <20 years old. |
It is more associated with Increase maternal age |
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Prematurity |
High gravid |
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It is not covered by peritoneum and amnion |
It is covered by amnion, Wharton jelly and peritoneum |
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It is a central defect |
It is situated usually right of umbilicus |
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Size of the opening < 5cm |
2-12 cm |
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Umbilical cord is situated at its central or little lateral in position of sac |
Umbilical cord is situated at its central and protruded content just right to it |
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Content : intestines, other organs including the stomach and liver protruded
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Content : usually content intestines, other organs including the liver, spleen
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10% cases with increase alpha feto protein level |
90% cases with increase alpha feto protein level |
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It is not associate with chromosomal abnormality or other birth defect like omphalocele so the survival rate is excellent
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It is associated with a high rate of mortality (25%) and severe malformations, such as cardiac anomalies (50%), neural tube defect (40%), exstrophy of the bladder and Beckwith–Wiedemann syndrom. Approximately 15% of live-born infants with omphalocele have chromosomal abnormalities. About 30% of infants with an omphalocele have other congenital abnormalities |
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During the fourth week of human embryonic development , the lateral body wall folds of the embryo meet at the midline and fuse together to form the anterior body wall. However, in gastroschisis and other anterior body wall defects, this fails to occur by either one or both of the lateral body wall folds not moving properly to meet with the other and fusing together This incomplete fusion results in a defect that allows abdominal organs to protrude through the abdominal wall, and the intestines typically herniate through the rectus abdominis muscle, lying to the right of the umbilicus. |
Omphalocele is caused by malrotation of the bowels while returning to the abdomen during development. Some cases of omphalocele are believed to be due to an underlying genetic disorder, such as Edward's syndrome (trisomy 18) or Patau syndrome (trisomy 13). Beckwith–Wiedemann syndrome is also associated with omphaloceles.
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