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Results for “INTESTINAL ATRESIA”
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[A case of congenital multiple intestinal atresia, associated with a pancreatic deformity].
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[Case of agenesia of the valve of Bauhin with intestinal atresia].
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Pyloric obstruction, duodenal dilatation, and extrahepatic cholestasis: a neonatal triad suggesting multiple intestinal atresias.
Whereas physiologic jaundice constitutes a common finding in neonates, a few cases present with cholestatic jaundice owing to various pathologic conditions, including extrahepatic biliary obstruction. We report the case of a 2-day-old female neonate presenting with neonatal cholestasis, nonbilious vomiting with pyloric obstruction, and multiple intestinal atresias. A pathognomonic clinicoradiologic triad is described, based on clinical data, plain abdominal x-ray, and ultrasound examination.
An important step in management of intestinal atresia.
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Compensatory hypertrophy of the gut in an infant with intestinal atresia.
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The "solid stage" and congenital intestinal atresia.
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[Neonatal congenital intestinal atresia].
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Congenital intestinal atresia; a report of 17 cases.
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[Residual disorders of peristalsis after surgery of intestinal atresia. Therapeutic consequences. Study of 71 cases].
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[Small intestine atresia. 21 cases].
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[Apropos of 2 cases of neonatal occlusion caused by intestinal atresia].
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[Quantitative determinations of the enzymes in meconium in addition to the findings in intestines in intestinal atresia and pancreatic fibrosis].
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[Intestinal atresia; study of 17 cases].
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Experimental intestinal atresia.
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Population-based study of small intestinal atresia and stenosis, Hawaii, 1986-2000.
Atresia and stenosis are some of the most common birth defects affecting the small intestine. Few population-based studies have examined the epidemiology of small intestinal atresia/stenosis. Eighty-two cases of small intestinal atresia/stenosis were identified through a population-based birth defects registry in Hawaii during 1986-2000. The relationships of various clinical and demographic factors with small intestinal atresia/stenosis and duodenal atresia/stenosis were examined. The small intestinal atresia/stenosis and duodenal atresia/stenosis rates were 2.9 per 10,000 live births [95% confidence interval (CI) 2.3-3.6] and 1.3 per 10,000 live births (95% CI 1.0-1.9), respectively. No secular trend was observed (P = 0.067 and 0.090, respectively). Maternal age risk for small intestinal atresia/stenosis was U-shaped, while duodenal atresia/stenosis rates were highest with maternal age of 35 years or more. Small intestinal atresia/stenosis was substantially more common among Far East Asians than Caucasians [rate ratio (RR) 1.96, 95% CI 1.24-2.94]. Duodenal atresia/stenosis risk was higher in Hawaii County than in Honolulu County (RR 2.55, 95% CI 1.10-5.02). Small intestinal atresia/stenosis was also associated with low birth weight (RR 11.50, 95% CI 8.05-15.92), low gestational age (RR 8.60, 95% CI 6.34-11.41) and multiple births (RR 3.79, 95% CI 1.39-8.24). In conclusion, this study found associations between small intestinal atresia/stenosis and maternal age, maternal race/ethnicity, county of residence, birth weight, gestational age and plurality, but not delivery period. Many of the associations between small intestinal atresia/stenosis and other factors noted in this investigation were similar to those reported by other studies.
Congenital intestinal atresia.
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