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Gastroschisis



Gastroschisis
Classification & external resources
Sagittal view
ICD-10 Q79.3
OMIM 230750
DiseasesDB 31155
MedlinePlus 000992
eMedicine ped/1642  radio/303
MeSH D020139

Gastroschisis is a type of abdominal wall defect in which the intestines and sometimes other organs develop outside the fetal abdomen through an opening in the abdominal wall. This defect is the result of obstruction of the omphalomesenteric vessels during development. It is often detected through AFP screening or a detailed fetal ultrasound. Gastroschisis is also called paraomphalocele, laparoschisis, or abdominoschisis.

Omphalocele is a similar birth defect, but it involves the umbilical cord, and the organs are enclosed in a membranous sac instead of directly in the amniotic fluid.

Genetic counseling and further genetic testing, such as amniocentesis, may be offered during the pregnancy, as some abdominal wall defects are associated with genetic disorders. If there are no additional genetic problems or birth defects, surgery soon after birth can often repair the opening.

Additional recommended knowledge

Contents

Embryology

During the fourth week of development, the lateral body folds move ventrally and fuse in the midline to form the anterior body wall. Incomplete fusion results in a defect that allows abdominal viscera to protrude through the abdominal wall. The bowel typically herniates through the rectus muscle, lying to the right of the umbilicus.

Mortality and Morbidity

Current advances in surgical techniques and intensive care management for neonates have increased the survival rate to 90%, in adequate settings. The possibility of prenatal diagnosis either through echosonogram or any other method available allows the mother to be referred to an adequate center where a caesarean section can be made at term (or as close to full term as possible) and allow the immediate surgery to be performed in the newborn. The morbidity is closely related to the presence of other malformations and complications of the wound or the intestine. Patients frequently require more than one surgery.

Statistics

The malformation is slightly more frequent in males than females. The frequency of gastroschisis is associated with young maternal age, and low number of gestations.

It has been reported that the incidence of gastroschisis has increased in recent years.[1]

Causes and Risk Factors

High-risk pregnancies such as those complicated by infection, young maternal age, smoking, drug abuse, or anything that contributes to low birth weight can increase the incidence of gastroschisis, which is more frequent in newborns who are small for gestational age. Whether the intrauterine growth retardation can facilitate the apparition of gastroschisis or the abdominal wall defect impairs fetal growth is not clear yet.

A change in paternity (childbearing with different fathers) has been implicated as a risk factor in a recent study, suggesting that the immune system of the mother may play a role in the development of gastroschisis.[2]

References

  1. ^ Feldkamp ML, Carey JC, Sadler TW (2007). "Development of gastroschisis: review of hypotheses, a novel hypothesis, and implications for research". Am. J. Med. Genet. A 143 (7): 639–52. doi:10.1002/ajmg.a.31578. PMID 17230493.
  2. ^ Chambers CD, Chen BH, Kalla K, Jernigan L, Jones KL (2007). "Novel risk factor in gastroschisis: change of paternity". Am. J. Med. Genet. A 143 (7): 653–9. doi:10.1002/ajmg.a.31577. PMID 17163540.


 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Gastroschisis". A list of authors is available in Wikipedia.
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