Results 191 to 200 of about 12,598 (246)

Congenital duodenal obstruction: A 32-year review

Journal of Pediatric Surgery, 1993
Although survival in infants with congenital intestinal obstruction has improved, duodenal obstruction continues to present unique challenges. One hundred thirty-eight newborns and infants (aged 0 to 30 days) were treated for congenital duodenal obstruction. Sixty-five were boys and 73 were girls. Sixty-one (45%) were premature.
P V, Bailey, T F, Tracy, R H, Connors, D P, Mooney, J E, Lewis, T R, Weber   +5 more
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Congenital duodenal obstruction: causes and imaging approach

Pediatric Radiology, 2016
Bilious emesis is a common cause for evaluation in pediatric radiology departments. There are several causes of congenital duodenal obstruction, most of which require elective surgical correction, but the potential of malrotation with midgut volvulus demands prompt imaging evaluation. We review the various causes of congenital duodenal obstruction with
Michael F, Brinkley, Elisabeth T, Tracy, Charles M, Maxfield   +2 more
openaire   +4 more sources

CONGENITAL DUODENAL OBSTRUCTION (INTRINSIC OBSTRUCTION)

Archives of Surgery, 1948
CONGENITAL atresia and stenosis of the intestinal tract of infants have been associated with a high mortality rate. In 1922 Davis and Poynter 1 collected 392 cases. The mortality was 100 per cent for congenital occlusive lesions of the intestines between the pylorus and the rectum.
C D, BENSON, G C, PENBERTHY
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Congenital Duodenal Obstruction

The British Journal of Radiology, 1941
(1) A short description of congenital duodenal obstruction is given. (2) A case with unusual findings is described.
  +4 more sources

CONGENITAL DUODENAL OBSTRUCTION

American Journal of Diseases of Children, 1946
IN recent years there has been a significant improvement in the results of the surgical management of congenital duodenal obstruction. In November 1945 Swenson and Ladd 1 reported 21 cases of intrinsic duodenal obstruction in the newborn, with 13 recoveries after operation.
H Z, MELLINS, D H, MILMAN
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Study of congenital duodenal obstruction

The Indian Journal of Pediatrics, 1995
A study of 23 neonates with congenital duodenal obstruction is reported. Their mean gestational age was 38 weeks and mean weight was 2.2 kg. Main clinical features observed were vomiting (100%), which was bilious in 74%, and epigastric fullness with visible peristalsis (74%). Plain X-ray abdomen confirmed the diagnosis in 78%.
K N, Rattan, A, Sharma, V K, Sharma
openaire   +2 more sources

Laparoscopic Repair of Congenital Duodenal Obstruction

Journal of Laparoendoscopic & Advanced Surgical Techniques, 2006
CHARGE syndrome (or association) refers to a group of physical abnormalities occurring together: coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, and ear anomalies/deafness. We report the successful use of laparoscopy in a patient with CHARGE syndrome and congenital duodenal obstruction.
Constantine T, Frantzides, Atul K, Madan, Punj K, Gupta, Claire, Smith, Ali, Keshavarzian   +4 more
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Radiological assessment of duodenal calibre in congenital duodenal obstruction

Pediatric Radiology, 1992
A review of barium meal studies in 32 cases of congenital intrinsic duodenal obstruction (CDO) from the Adelaide Children's Hospital was performed to assess and measure pre and post operative duodenal dilatation. Comparisons were made with a group of 153 normal barium studies from the same Hospital with a view to quantifying normal and abnormal ...
R J, Linke, L L, Morris, R P, Davies, T M, Cain, R B, Davey   +4 more
openaire   +2 more sources

Congenital Duodenal Obstruction

2014
Congenital duodenal atresia is a congenital bowel obstruction, usually affecting the second part of duodenum. The overall incidence is about one in 6000 births. Approximately one-third of patients with duodenal obstruction have trisomy 21 (Down’s syndrome).
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