Results 261 to 270 of about 22,210 (303)
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Small Intestinal Atresia

2019
If not diagnosed antenally, small intestinal atresia usually presents as bilious vomiting, abdominal distention and failure to pass meconium. Dilated loops of bowel without distal air on abdominal x-ray is highly suggestive of small bowel atresia. These patients are often treated with bowel resection and end-to-end anastomosis. This chapter talks about
Todd A. Ponsky   +2 more
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Intestinal plication in the treatment of atresia

Journal of Pediatric Surgery, 1983
Twelve infants with jejunal atresia were managed by plication of the dilated proximal bowel and end-to-oblique anastomosis. The technique is simple and very effective in preventing functional obstruction of the dilated bowel, and it preserves the mucosal absorptive surface.
Michael R. Harrison   +1 more
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Gastroschisis and Total Intestinal Atresia

European Journal of Pediatric Surgery, 1998
Gastroschisis is an uncommon condition which is now being detected at an earlier stage due to the use of routine antenatal ultrasound scanning. The presence of intestinal atresia secondary to impairment of the vascular supply is well recognised and is associated with a poorer outcome because of the potential for loss of bowel length.
G. Morris-Stiff, J. Lari, A. Al-Wafi
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CONGENITAL ATRESIA OF THE INTESTINE

Archives of Pediatrics & Adolescent Medicine, 1929
Although rare, congenital atresia of the intestine occurs with sufficient frequency to be of clinical importance. Calder 1 first called attention to this condition in 1733, and case reports, discussions of etiology, symptomatology and treatment have appeared at intervals since, more frequently during the past quarter century. Attention should be called
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Origin of Intestinal Atresia of Newborn

JAMA, 1964
Current concepts of the pathogenesis of intestinal atresia of the newborn cast considerable doubt on the classical theory of failure of recanalization. Clinical and experimental evidence make it probable that atresias are the consequence of intrauterine abdominal catastrophes occurring late in fetal life.
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CONGENITAL INTESTINAL ATRESIA

Archives of Pediatrics & Adolescent Medicine, 1931
Congenital atresia and stenosis of the intestine, exclusive of the pylorus, rectum and anal canal, is a relatively rare condition, occurring in about 1 of 20,000 infants. We have been able to find mention of more than 500 instances previously reported in the literature, though this number probably does not include all the recorded cases.
C. H. Webb, Owen H. Wangensteen
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Intestinal Atresia

2010
Milestones in Pediatric Surgery.- Milestones in Pediatric Surgery.- Principles of Surgical Science.- Fluids, Electrolytes, and Dehydration.- Metabolic Response to Injury and Sepsis.- Shock.- Parenteral Nutrition.- Hematology for Surgeons.- Postoperative Problems.- Neonatal Physiology and Care.- Fetal and Neonatal Surgery.- Fetal Surgery: General ...
Sinha, Chandrasen K.   +2 more
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Intestinal Atresia

Archives of Surgery, 1968
G, Dykstra   +2 more
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Atresia of the Small Intestine

Southern Medical Journal, 1969
Levy Jl, Linder Lh
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Congenital atresia of the small intestine

The American Journal of Surgery, 1962
Abstract Congenital atresia of the small intestine is rare, uniformly fatal if untreated and demands early diagnosis and careful preoperative preparation. Corrective surgery must be precise, designed to remedy the lesion in a single procedure and conducted with careful attention to blood replacement and maintenance of body warmth.
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