Duodenal atresia history and symptoms

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]

Overview

The hallmark of duodenal atresia is bilious emesis with in the first 48 hours of life. A positive history of persistent emesis and feeding difficulties is suggestive of duodenal atresia. The most common symptoms of duodenal atresia include bilious emesis, persistent emesis, and feeding difficulties.

History and Symptoms

The history and symptoms of duodenal atresia is as follows:^[1]^[2]

The hallmark of duodenal atresia is bilious vomiting.
A positive history of persistent emesis and feeding difficulty is suggestive of duodenal atresia.

History

Patients with duodenal atresia may have a positive history of:

Persistent vomiting
Bilious emesis
Feeding difficulties

Common Symptoms

Common symptoms of duodenal atresia include:

Bilious emesis
Feeding difficulties

Less Common Symptoms

Less common symptoms of duodenal atresia include:

Abdominal distention

References

↑ Freeman, SB; Torfs, CP; Romitti, PA; Royle, MH; Druschel, C; Hobbs, CA; Sherman, SL (2009). "Congenital gastrointestinal defects in Down syndrome: a report from the Atlanta and National Down Syndrome Projects". Clinical Genetics. 75 (2): 180–184. doi:10.1111/j.1399-0004.2008.01110.x. ISSN 0009-9163.
↑ Morris, Grant; Kennedy, Alfred; Cochran, William (2016). "Small Bowel Congenital Anomalies: a Review and Update". Current Gastroenterology Reports. 18 (4). doi:10.1007/s11894-016-0490-4. ISSN 1522-8037.

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[FreemanTorfs2009-1] Freeman, SB; Torfs, CP; Romitti, PA; Royle, MH; Druschel, C; Hobbs, CA; Sherman, SL (2009). "Congenital gastrointestinal defects in Down syndrome: a report from the Atlanta and National Down Syndrome Projects". Clinical Genetics. 75 (2): 180–184. doi:10.1111/j.1399-0004.2008.01110.x. ISSN 0009-9163.

[MorrisKennedy2016-2] Morris, Grant; Kennedy, Alfred; Cochran, William (2016). "Small Bowel Congenital Anomalies: a Review and Update". Current Gastroenterology Reports. 18 (4). doi:10.1007/s11894-016-0490-4. ISSN 1522-8037.

[1]

[2]