Abstract
A duodenal obstruction with three separate obstructing duodenal webs is a very rare congenital anomaly, with only one other case reported in the literature. We present a case in a 3-week-old newborn that underwent successful surgical repair.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 30-33 |
| Number of pages | 4 |
| Journal | Journal of Pediatric Surgery Case Reports |
| Volume | 8 |
| DOIs | |
| Publication status | Published - May 2016 |
| Externally published | Yes |
Keywords
- Duodenal atresia
- Malrotation
- Triple
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