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- W1648651788 abstract "Background and Purpose: In contrast to other malformations, congenital anomalies of the gastrointestinal (GI) tract have scarcely been investigated. The purpose of this study was to evaluate the characteristics of congenital GI obstruction in young infants in the past 6 years at a general hospital in Taiwan. Methods: Medical charts of 35 patients diagnosed with congenital GI obstruction during January 1998 to July 2004 were reviewed. Results: A congenital GI anomaly which caused alimentary tract obstruction included idiopathic hypertrophic pyloric stenosis (IHPS) in 16 (46%), an imperforate anus in 5 (14%), malrotation in 4 (11%), Hirschsprung disease in 4 (11%), ileal atresia in 3 (9%), an annular pancreas in 2 (6%), and esophageal atresia with a distal tracheoesophageal fistula in 1 (3%). The male/female ratio was to 2.89/1. The most common presenting sign or symptom was abdominal distension (93%), followed by non-bilious vomiting (59%) and bilious vomiting (31%). All patients survived. Conclusions: Infants with unexplained GI symptoms must be examined for the possibility of congenital anomalies of the GI tract. The most common congenital GI malformation is IHPS. Conventional radiology is still extremely useful in diagnosing digestive tract anomalies." @default.
- W1648651788 created "2016-06-24" @default.
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- W1648651788 date "2007-09-01" @default.
- W1648651788 modified "2023-09-24" @default.
- W1648651788 title "Congenital Gastrointestinal Anomalies Producing Gastrointestinal Obstruction in Infants" @default.
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